Canonical Allele Identifier: CA376071601

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828315C>G (hg19) ; chr10:g.18539386C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539386C>G , CM000672.2:g.18539386C>G	GRCh38
NC_000010.10:g.18828315C>G , CM000672.1:g.18828315C>G	GRCh37
NC_000010.9:g.18868321C>G	NCBI36
NG_016195.1:g.403710C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1501C>G (CACNB2)	ENSP00000366532.4:p.Leu501Val
ENST00000377319.9:c.1366C>G (CACNB2)	ENSP00000366536.3:p.Leu456Val
ENST00000645287.2:c.1489C>G (CACNB2)	ENSP00000496203.1:p.Leu497Val
ENST00000282343.13:c.1561C>G (CACNB2)	ENSP00000282343.8:p.Leu521Val
ENST00000324631.13:c.1645C>G (CACNB2) MANE Select	ENSP00000320025.8:p.Leu549Val
ENST00000377315.5:c.1501C>G (CACNB2)	ENSP00000366532.4:p.Leu501Val
ENST00000377319.8:c.1366C>G (CACNB2)	ENSP00000366536.3:p.Leu456Val
ENST00000377329.10:c.1483C>G (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Leu495Val
ENST00000377331.8:c.1270C>G (CACNB2)	ENSP00000366548.4:p.Leu424Val
ENST00000643096.2:c.1447C>G (CACNB2)	ENSP00000494209.2:p.Leu483Val
ENST00000645287.1:c.1489C>G (CACNB2)	ENSP00000496203.1:p.Leu497Val
ENST00000647168.2:c.*786C>G (CACNB2)	ENSP00000495854.2:n.*786C>G
ENST00000650685.1:c.1387C>G (CACNB2)	ENSP00000498460.1:p.Leu463Val
ENST00000651330.1:c.*919C>G (CACNB2)	ENSP00000498457.1:n.*919C>G
ENST00000651468.1:c.1202C>G (CACNB2)	ENSP00000498352.1:n.1202C>G
ENST00000651928.1:c.*884C>G (CACNB2)	ENSP00000499177.1:n.*884C>G
ENST00000652391.1:c.1465C>G (CACNB2)	ENSP00000498938.1:p.Leu489Val
ENST00000652478.1:c.*745C>G (CACNB2)	ENSP00000498812.1:n.*745C>G
ENST00000282343.12:c.1561C>G (CACNB2)	ENSP00000282343.8:p.Leu521Val
ENST00000324631.11:c.1645C>G (CACNB2)	ENSP00000320025.7:p.Leu549Val
ENST00000352115.10:c.1573C>G (CACNB2)	ENSP00000344474.6:p.Leu525Val
ENST00000377315.4:c.1501C>G (CACNB2)	ENSP00000366532.4:p.Leu501Val
ENST00000377319.7:c.1366C>G (CACNB2)	ENSP00000366536.3:p.Leu456Val
ENST00000377328.5:c.895C>G (CACNB2)	ENSP00000366545.1:p.Leu299Val
ENST00000377329.8:c.1483C>G (CACNB2)	ENSP00000366546.4:p.Leu495Val
ENST00000377331.6:c.1489C>G (CACNB2)	ENSP00000366548.2:p.Leu497Val
ENST00000396576.6:c.1480C>G (CACNB2)	ENSP00000379821.2:p.Leu494Val
ENST00000612134.4:c.1349C>G (CACNB2)	ENSP00000480563.1:n.1349C>G
ENST00000612743.1:c.157C>G (CACNB2)	ENSP00000478676.1:p.Leu53Val
ENST00000615785.4:c.730C>G (CACNB2)	ENSP00000480260.1:p.Leu244Val
ENST00000617363.4:c.1408C>G (CACNB2)	ENSP00000479756.1:p.Leu470Val
NM_000724.3:c.1480C>G (CACNB2)	NP_000715.2:p.Leu494Val
NM_001167945.1:c.1447C>G (CACNB2)	NP_001161417.1:p.Leu483Val
NM_201570.2:c.1501C>G (CACNB2)	NP_963864.1:p.Leu501Val
NM_201571.3:c.1561C>G (CACNB2)	NP_963865.2:p.Leu521Val
NM_201572.3:c.1489C>G (CACNB2)	NP_963866.2:p.Leu497Val
NM_201590.2:c.1483C>G (CACNB2)	NP_963884.2:p.Leu495Val
NM_201593.2:c.1531C>G (CACNB2)	NP_963887.2:p.Leu511Val
NM_201596.2:c.1645C>G (CACNB2)	NP_963890.2:p.Leu549Val
NM_201597.2:c.1573C>G (CACNB2)	NP_963891.1:p.Leu525Val
XM_005252588.2:c.1387C>G (CACNB2)	XP_005252645.1:p.Leu463Val
XM_005252591.2:c.805C>G (CACNB2)	XP_005252648.1:p.Leu269Val
XM_006717502.2:c.1465C>G (CACNB2)	XP_006717565.1:p.Leu489Val
XM_011519659.1:c.1411C>G (CACNB2)	XP_011517961.1:p.Leu471Val
XM_011519660.1:c.1366C>G (CACNB2)	XP_011517962.1:p.Leu456Val
NM_001330060.1:c.1366C>G (CACNB2)	NP_001316989.1:p.Leu456Val
XM_005252588.4:c.1387C>G (CACNB2)	XP_005252645.1:p.Leu463Val
XM_005252591.3:c.805C>G (CACNB2)	XP_005252648.1:p.Leu269Val
XM_006717502.3:c.1465C>G (CACNB2)	XP_006717565.1:p.Leu489Val
XM_011519659.2:c.1411C>G (CACNB2)	XP_011517961.1:p.Leu471Val
XM_017016625.1:c.805C>G (CACNB2)	XP_016872114.1:p.Leu269Val
XR_001747060.1:n.2423+2683G>C (NSUN6)
XR_001747198.1:n.1770C>G (CACNB2)
NM_000724.4:c.1480C>G (CACNB2)	NP_000715.2:p.Leu494Val
NM_001167945.2:c.1447C>G (CACNB2)	NP_001161417.1:p.Leu483Val
NM_001330060.2:c.1366C>G (CACNB2)	NP_001316989.1:p.Leu456Val
NM_201570.3:c.1501C>G (CACNB2)	NP_963864.1:p.Leu501Val
NM_201571.4:c.1561C>G (CACNB2)	NP_963865.2:p.Leu521Val
NM_201572.4:c.1489C>G (CACNB2)	NP_963866.2:p.Leu497Val
NM_201590.3:c.1483C>G (CACNB2) MANE Plus Clinical	NP_963884.2:p.Leu495Val
NM_201593.3:c.1531C>G (CACNB2)	NP_963887.2:p.Leu511Val
NM_201596.3:c.1645C>G (CACNB2) MANE Select	NP_963890.2:p.Leu549Val
NM_201597.3:c.1573C>G (CACNB2)	NP_963891.1:p.Leu525Val