Canonical Allele Identifier: CA376071737

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828352A>T (hg19) ; chr10:g.18539423A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539423A>T , CM000672.2:g.18539423A>T	GRCh38
NC_000010.10:g.18828352A>T , CM000672.1:g.18828352A>T	GRCh37
NC_000010.9:g.18868358A>T	NCBI36
NG_016195.1:g.403747A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1538A>T (CACNB2)	ENSP00000366532.4:p.Glu513Val
ENST00000377319.9:c.1403A>T (CACNB2)	ENSP00000366536.3:p.Glu468Val
ENST00000645287.2:c.1526A>T (CACNB2)	ENSP00000496203.1:p.Glu509Val
ENST00000282343.13:c.1598A>T (CACNB2)	ENSP00000282343.8:p.Glu533Val
ENST00000324631.13:c.1682A>T (CACNB2) MANE Select	ENSP00000320025.8:p.Glu561Val
ENST00000377315.5:c.1538A>T (CACNB2)	ENSP00000366532.4:p.Glu513Val
ENST00000377319.8:c.1403A>T (CACNB2)	ENSP00000366536.3:p.Glu468Val
ENST00000377329.10:c.1520A>T (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Glu507Val
ENST00000377331.8:c.1307A>T (CACNB2)	ENSP00000366548.4:p.Glu436Val
ENST00000643096.2:c.1484A>T (CACNB2)	ENSP00000494209.2:p.Glu495Val
ENST00000645287.1:c.1526A>T (CACNB2)	ENSP00000496203.1:p.Glu509Val
ENST00000647168.2:c.*823A>T (CACNB2)	ENSP00000495854.2:n.*823A>T
ENST00000650685.1:c.1424A>T (CACNB2)	ENSP00000498460.1:p.Glu475Val
ENST00000651330.1:c.*956A>T (CACNB2)	ENSP00000498457.1:n.*956A>T
ENST00000651468.1:c.1239A>T (CACNB2)	ENSP00000498352.1:n.1239A>T
ENST00000651928.1:c.*921A>T (CACNB2)	ENSP00000499177.1:n.*921A>T
ENST00000652391.1:c.1502A>T (CACNB2)	ENSP00000498938.1:p.Glu501Val
ENST00000652478.1:c.*782A>T (CACNB2)	ENSP00000498812.1:n.*782A>T
ENST00000282343.12:c.1598A>T (CACNB2)	ENSP00000282343.8:p.Glu533Val
ENST00000324631.11:c.1682A>T (CACNB2)	ENSP00000320025.7:p.Glu561Val
ENST00000352115.10:c.1610A>T (CACNB2)	ENSP00000344474.6:p.Glu537Val
ENST00000377315.4:c.1538A>T (CACNB2)	ENSP00000366532.4:p.Glu513Val
ENST00000377319.7:c.1403A>T (CACNB2)	ENSP00000366536.3:p.Glu468Val
ENST00000377328.5:c.932A>T (CACNB2)	ENSP00000366545.1:p.Glu311Val
ENST00000377329.8:c.1520A>T (CACNB2)	ENSP00000366546.4:p.Glu507Val
ENST00000377331.6:c.1526A>T (CACNB2)	ENSP00000366548.2:p.Glu509Val
ENST00000396576.6:c.1517A>T (CACNB2)	ENSP00000379821.2:p.Glu506Val
ENST00000612134.4:c.1386A>T (CACNB2)	ENSP00000480563.1:n.1386A>T
ENST00000612743.1:c.194A>T (CACNB2)	ENSP00000478676.1:p.Glu65Val
ENST00000615785.4:c.767A>T (CACNB2)	ENSP00000480260.1:p.Glu256Val
ENST00000617363.4:c.1445A>T (CACNB2)	ENSP00000479756.1:p.Glu482Val
NM_000724.3:c.1517A>T (CACNB2)	NP_000715.2:p.Glu506Val
NM_001167945.1:c.1484A>T (CACNB2)	NP_001161417.1:p.Glu495Val
NM_201570.2:c.1538A>T (CACNB2)	NP_963864.1:p.Glu513Val
NM_201571.3:c.1598A>T (CACNB2)	NP_963865.2:p.Glu533Val
NM_201572.3:c.1526A>T (CACNB2)	NP_963866.2:p.Glu509Val
NM_201590.2:c.1520A>T (CACNB2)	NP_963884.2:p.Glu507Val
NM_201593.2:c.1568A>T (CACNB2)	NP_963887.2:p.Glu523Val
NM_201596.2:c.1682A>T (CACNB2)	NP_963890.2:p.Glu561Val
NM_201597.2:c.1610A>T (CACNB2)	NP_963891.1:p.Glu537Val
XM_005252588.2:c.1424A>T (CACNB2)	XP_005252645.1:p.Glu475Val
XM_005252591.2:c.842A>T (CACNB2)	XP_005252648.1:p.Glu281Val
XM_006717502.2:c.1502A>T (CACNB2)	XP_006717565.1:p.Glu501Val
XM_011519659.1:c.1448A>T (CACNB2)	XP_011517961.1:p.Glu483Val
XM_011519660.1:c.1403A>T (CACNB2)	XP_011517962.1:p.Glu468Val
NM_001330060.1:c.1403A>T (CACNB2)	NP_001316989.1:p.Glu468Val
XM_005252588.4:c.1424A>T (CACNB2)	XP_005252645.1:p.Glu475Val
XM_005252591.3:c.842A>T (CACNB2)	XP_005252648.1:p.Glu281Val
XM_006717502.3:c.1502A>T (CACNB2)	XP_006717565.1:p.Glu501Val
XM_011519659.2:c.1448A>T (CACNB2)	XP_011517961.1:p.Glu483Val
XM_017016625.1:c.842A>T (CACNB2)	XP_016872114.1:p.Glu281Val
XR_001747060.1:n.2423+2646T>A (NSUN6)
XR_001747198.1:n.1807A>T (CACNB2)
NM_000724.4:c.1517A>T (CACNB2)	NP_000715.2:p.Glu506Val
NM_001167945.2:c.1484A>T (CACNB2)	NP_001161417.1:p.Glu495Val
NM_001330060.2:c.1403A>T (CACNB2)	NP_001316989.1:p.Glu468Val
NM_201570.3:c.1538A>T (CACNB2)	NP_963864.1:p.Glu513Val
NM_201571.4:c.1598A>T (CACNB2)	NP_963865.2:p.Glu533Val
NM_201572.4:c.1526A>T (CACNB2)	NP_963866.2:p.Glu509Val
NM_201590.3:c.1520A>T (CACNB2) MANE Plus Clinical	NP_963884.2:p.Glu507Val
NM_201593.3:c.1568A>T (CACNB2)	NP_963887.2:p.Glu523Val
NM_201596.3:c.1682A>T (CACNB2) MANE Select	NP_963890.2:p.Glu561Val
NM_201597.3:c.1610A>T (CACNB2)	NP_963891.1:p.Glu537Val