Canonical Allele Identifier: CA376071631

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828324C>G (hg19) ; chr10:g.18539395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539395C>G , CM000672.2:g.18539395C>G	GRCh38
NC_000010.10:g.18828324C>G , CM000672.1:g.18828324C>G	GRCh37
NC_000010.9:g.18868330C>G	NCBI36
NG_016195.1:g.403719C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1510C>G (CACNB2)	ENSP00000366532.4:p.Gln504Glu
ENST00000377319.9:c.1375C>G (CACNB2)	ENSP00000366536.3:p.Gln459Glu
ENST00000645287.2:c.1498C>G (CACNB2)	ENSP00000496203.1:p.Gln500Glu
ENST00000282343.13:c.1570C>G (CACNB2)	ENSP00000282343.8:p.Gln524Glu
ENST00000324631.13:c.1654C>G (CACNB2) MANE Select	ENSP00000320025.8:p.Gln552Glu
ENST00000377315.5:c.1510C>G (CACNB2)	ENSP00000366532.4:p.Gln504Glu
ENST00000377319.8:c.1375C>G (CACNB2)	ENSP00000366536.3:p.Gln459Glu
ENST00000377329.10:c.1492C>G (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Gln498Glu
ENST00000377331.8:c.1279C>G (CACNB2)	ENSP00000366548.4:p.Gln427Glu
ENST00000643096.2:c.1456C>G (CACNB2)	ENSP00000494209.2:p.Gln486Glu
ENST00000645287.1:c.1498C>G (CACNB2)	ENSP00000496203.1:p.Gln500Glu
ENST00000647168.2:c.*795C>G (CACNB2)	ENSP00000495854.2:n.*795C>G
ENST00000650685.1:c.1396C>G (CACNB2)	ENSP00000498460.1:p.Gln466Glu
ENST00000651330.1:c.*928C>G (CACNB2)	ENSP00000498457.1:n.*928C>G
ENST00000651468.1:c.1211C>G (CACNB2)	ENSP00000498352.1:n.1211C>G
ENST00000651928.1:c.*893C>G (CACNB2)	ENSP00000499177.1:n.*893C>G
ENST00000652391.1:c.1474C>G (CACNB2)	ENSP00000498938.1:p.Gln492Glu
ENST00000652478.1:c.*754C>G (CACNB2)	ENSP00000498812.1:n.*754C>G
ENST00000282343.12:c.1570C>G (CACNB2)	ENSP00000282343.8:p.Gln524Glu
ENST00000324631.11:c.1654C>G (CACNB2)	ENSP00000320025.7:p.Gln552Glu
ENST00000352115.10:c.1582C>G (CACNB2)	ENSP00000344474.6:p.Gln528Glu
ENST00000377315.4:c.1510C>G (CACNB2)	ENSP00000366532.4:p.Gln504Glu
ENST00000377319.7:c.1375C>G (CACNB2)	ENSP00000366536.3:p.Gln459Glu
ENST00000377328.5:c.904C>G (CACNB2)	ENSP00000366545.1:p.Gln302Glu
ENST00000377329.8:c.1492C>G (CACNB2)	ENSP00000366546.4:p.Gln498Glu
ENST00000377331.6:c.1498C>G (CACNB2)	ENSP00000366548.2:p.Gln500Glu
ENST00000396576.6:c.1489C>G (CACNB2)	ENSP00000379821.2:p.Gln497Glu
ENST00000612134.4:c.1358C>G (CACNB2)	ENSP00000480563.1:n.1358C>G
ENST00000612743.1:c.166C>G (CACNB2)	ENSP00000478676.1:p.Gln56Glu
ENST00000615785.4:c.739C>G (CACNB2)	ENSP00000480260.1:p.Gln247Glu
ENST00000617363.4:c.1417C>G (CACNB2)	ENSP00000479756.1:p.Gln473Glu
NM_000724.3:c.1489C>G (CACNB2)	NP_000715.2:p.Gln497Glu
NM_001167945.1:c.1456C>G (CACNB2)	NP_001161417.1:p.Gln486Glu
NM_201570.2:c.1510C>G (CACNB2)	NP_963864.1:p.Gln504Glu
NM_201571.3:c.1570C>G (CACNB2)	NP_963865.2:p.Gln524Glu
NM_201572.3:c.1498C>G (CACNB2)	NP_963866.2:p.Gln500Glu
NM_201590.2:c.1492C>G (CACNB2)	NP_963884.2:p.Gln498Glu
NM_201593.2:c.1540C>G (CACNB2)	NP_963887.2:p.Gln514Glu
NM_201596.2:c.1654C>G (CACNB2)	NP_963890.2:p.Gln552Glu
NM_201597.2:c.1582C>G (CACNB2)	NP_963891.1:p.Gln528Glu
XM_005252588.2:c.1396C>G (CACNB2)	XP_005252645.1:p.Gln466Glu
XM_005252591.2:c.814C>G (CACNB2)	XP_005252648.1:p.Gln272Glu
XM_006717502.2:c.1474C>G (CACNB2)	XP_006717565.1:p.Gln492Glu
XM_011519659.1:c.1420C>G (CACNB2)	XP_011517961.1:p.Gln474Glu
XM_011519660.1:c.1375C>G (CACNB2)	XP_011517962.1:p.Gln459Glu
NM_001330060.1:c.1375C>G (CACNB2)	NP_001316989.1:p.Gln459Glu
XM_005252588.4:c.1396C>G (CACNB2)	XP_005252645.1:p.Gln466Glu
XM_005252591.3:c.814C>G (CACNB2)	XP_005252648.1:p.Gln272Glu
XM_006717502.3:c.1474C>G (CACNB2)	XP_006717565.1:p.Gln492Glu
XM_011519659.2:c.1420C>G (CACNB2)	XP_011517961.1:p.Gln474Glu
XM_017016625.1:c.814C>G (CACNB2)	XP_016872114.1:p.Gln272Glu
XR_001747060.1:n.2423+2674G>C (NSUN6)
XR_001747198.1:n.1779C>G (CACNB2)
NM_000724.4:c.1489C>G (CACNB2)	NP_000715.2:p.Gln497Glu
NM_001167945.2:c.1456C>G (CACNB2)	NP_001161417.1:p.Gln486Glu
NM_001330060.2:c.1375C>G (CACNB2)	NP_001316989.1:p.Gln459Glu
NM_201570.3:c.1510C>G (CACNB2)	NP_963864.1:p.Gln504Glu
NM_201571.4:c.1570C>G (CACNB2)	NP_963865.2:p.Gln524Glu
NM_201572.4:c.1498C>G (CACNB2)	NP_963866.2:p.Gln500Glu
NM_201590.3:c.1492C>G (CACNB2) MANE Plus Clinical	NP_963884.2:p.Gln498Glu
NM_201593.3:c.1540C>G (CACNB2)	NP_963887.2:p.Gln514Glu
NM_201596.3:c.1654C>G (CACNB2) MANE Select	NP_963890.2:p.Gln552Glu
NM_201597.3:c.1582C>G (CACNB2)	NP_963891.1:p.Gln528Glu