Canonical Allele Identifier: CA2608435625

Gene: CACNB2 NSUN6

Linked Data

• gnomAD v4: 10-18539432-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539435_18539436del , CM000672.2:g.18539435_18539436del	GRCh38
NC_000010.10:g.18828364_18828365del , CM000672.1:g.18828364_18828365del	GRCh37
NC_000010.9:g.18868370_18868371del	NCBI36
NG_016195.1:g.403759_403760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1550_1551del (CACNB2)	ENSP00000366532.4:p.Ser517CysfsTer12
ENST00000377319.9:c.1415_1416del (CACNB2)	ENSP00000366536.3:p.Ser472CysfsTer12
ENST00000645287.2:c.1538_1539del (CACNB2)	ENSP00000496203.1:p.Ser513CysfsTer12
ENST00000282343.13:c.1610_1611del (CACNB2)	ENSP00000282343.8:p.Ser537CysfsTer12
ENST00000324631.13:c.1694_1695del (CACNB2) MANE Select	ENSP00000320025.8:p.Ser565CysfsTer12
ENST00000377315.5:c.1550_1551del (CACNB2)	ENSP00000366532.4:p.Ser517CysfsTer12
ENST00000377319.8:c.1415_1416del (CACNB2)	ENSP00000366536.3:p.Ser472CysfsTer12
ENST00000377329.10:c.1532_1533del (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Ser511CysfsTer12
ENST00000377331.8:c.1319_1320del (CACNB2)	ENSP00000366548.4:p.Ser440CysfsTer12
ENST00000643096.2:c.1496_1497del (CACNB2)	ENSP00000494209.2:p.Ser499CysfsTer12
ENST00000645287.1:c.1538_1539del (CACNB2)	ENSP00000496203.1:p.Ser513CysfsTer12
ENST00000647168.2:c.*835_*836del (CACNB2)	ENSP00000495854.2:n.*835_*836del
ENST00000650685.1:c.1436_1437del (CACNB2)	ENSP00000498460.1:p.Ser479CysfsTer12
ENST00000651330.1:c.*968_*969del (CACNB2)	ENSP00000498457.1:n.*968_*969del
ENST00000651468.1:c.1251_1252del (CACNB2)	ENSP00000498352.1:n.1251_1252del
ENST00000651928.1:c.*933_*934del (CACNB2)	ENSP00000499177.1:n.*933_*934del
ENST00000652391.1:c.1514_1515del (CACNB2)	ENSP00000498938.1:p.Ser505CysfsTer12
ENST00000652478.1:c.*794_*795del (CACNB2)	ENSP00000498812.1:n.*794_*795del
ENST00000282343.12:c.1610_1611del (CACNB2)	ENSP00000282343.8:p.Ser537CysfsTer12
ENST00000324631.11:c.1694_1695del (CACNB2)	ENSP00000320025.7:p.Ser565CysfsTer12
ENST00000352115.10:c.1622_1623del (CACNB2)	ENSP00000344474.6:p.Ser541CysfsTer12
ENST00000377315.4:c.1550_1551del (CACNB2)	ENSP00000366532.4:p.Ser517CysfsTer12
ENST00000377319.7:c.1415_1416del (CACNB2)	ENSP00000366536.3:p.Ser472CysfsTer12
ENST00000377328.5:c.944_945del (CACNB2)	ENSP00000366545.1:p.Ser315CysfsTer12
ENST00000377329.8:c.1532_1533del (CACNB2)	ENSP00000366546.4:p.Ser511CysfsTer12
ENST00000377331.6:c.1538_1539del (CACNB2)	ENSP00000366548.2:p.Ser513CysfsTer12
ENST00000396576.6:c.1529_1530del (CACNB2)	ENSP00000379821.2:p.Ser510CysfsTer12
ENST00000612134.4:c.1398_1399del (CACNB2)	ENSP00000480563.1:n.1398_1399del
ENST00000612743.1:c.206_207del (CACNB2)	ENSP00000478676.1:p.Ser69CysfsTer12
ENST00000615785.4:c.779_780del (CACNB2)	ENSP00000480260.1:p.Ser260CysfsTer12
ENST00000617363.4:c.1457_1458del (CACNB2)	ENSP00000479756.1:p.Ser486CysfsTer12
NM_000724.3:c.1529_1530del (CACNB2)	NP_000715.2:p.Ser510CysfsTer12
NM_001167945.1:c.1496_1497del (CACNB2)	NP_001161417.1:p.Ser499CysfsTer12
NM_201570.2:c.1550_1551del (CACNB2)	NP_963864.1:p.Ser517CysfsTer12
NM_201571.3:c.1610_1611del (CACNB2)	NP_963865.2:p.Ser537CysfsTer12
NM_201572.3:c.1538_1539del (CACNB2)	NP_963866.2:p.Ser513CysfsTer12
NM_201590.2:c.1532_1533del (CACNB2)	NP_963884.2:p.Ser511CysfsTer12
NM_201593.2:c.1580_1581del (CACNB2)	NP_963887.2:p.Ser527CysfsTer12
NM_201596.2:c.1694_1695del (CACNB2)	NP_963890.2:p.Ser565CysfsTer12
NM_201597.2:c.1622_1623del (CACNB2)	NP_963891.1:p.Ser541CysfsTer12
XM_005252588.2:c.1436_1437del (CACNB2)	XP_005252645.1:p.Ser479CysfsTer12
XM_005252591.2:c.854_855del (CACNB2)	XP_005252648.1:p.Ser285CysfsTer12
XM_006717502.2:c.1514_1515del (CACNB2)	XP_006717565.1:p.Ser505CysfsTer12
XM_011519659.1:c.1460_1461del (CACNB2)	XP_011517961.1:p.Ser487CysfsTer12
XM_011519660.1:c.1415_1416del (CACNB2)	XP_011517962.1:p.Ser472CysfsTer12
NM_001330060.1:c.1415_1416del (CACNB2)	NP_001316989.1:p.Ser472CysfsTer12
XM_005252588.4:c.1436_1437del (CACNB2)	XP_005252645.1:p.Ser479CysfsTer12
XM_005252591.3:c.854_855del (CACNB2)	XP_005252648.1:p.Ser285CysfsTer12
XM_006717502.3:c.1514_1515del (CACNB2)	XP_006717565.1:p.Ser505CysfsTer12
XM_011519659.2:c.1460_1461del (CACNB2)	XP_011517961.1:p.Ser487CysfsTer12
XM_017016625.1:c.854_855del (CACNB2)	XP_016872114.1:p.Ser285CysfsTer12
XR_001747060.1:n.2423+2635_2423+2636del (NSUN6)
XR_001747198.1:n.1819_1820del (CACNB2)
NM_000724.4:c.1529_1530del (CACNB2)	NP_000715.2:p.Ser510CysfsTer12
NM_001167945.2:c.1496_1497del (CACNB2)	NP_001161417.1:p.Ser499CysfsTer12
NM_001330060.2:c.1415_1416del (CACNB2)	NP_001316989.1:p.Ser472CysfsTer12
NM_201570.3:c.1550_1551del (CACNB2)	NP_963864.1:p.Ser517CysfsTer12
NM_201571.4:c.1610_1611del (CACNB2)	NP_963865.2:p.Ser537CysfsTer12
NM_201572.4:c.1538_1539del (CACNB2)	NP_963866.2:p.Ser513CysfsTer12
NM_201590.3:c.1532_1533del (CACNB2) MANE Plus Clinical	NP_963884.2:p.Ser511CysfsTer12
NM_201593.3:c.1580_1581del (CACNB2)	NP_963887.2:p.Ser527CysfsTer12
NM_201596.3:c.1694_1695del (CACNB2) MANE Select	NP_963890.2:p.Ser565CysfsTer12
NM_201597.3:c.1622_1623del (CACNB2)	NP_963891.1:p.Ser541CysfsTer12