Canonical Allele Identifier: CA1894173192

Gene: CACNB2 NSUN6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539365C= , CM000672.2:g.18539365C=	GRCh38
NC_000010.10:g.18828294C= , CM000672.1:g.18828294C=	GRCh37
NC_000010.9:g.18868300C=	NCBI36
NG_016195.1:g.403689C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1480C= (CACNB2)	ENSP00000366532.4:p.Arg494=
ENST00000377319.9:c.1345C= (CACNB2)	ENSP00000366536.3:p.Arg449=
ENST00000645287.2:c.1468C= (CACNB2)	ENSP00000496203.1:p.Arg490=
ENST00000282343.13:c.1540C= (CACNB2)	ENSP00000282343.8:p.Arg514=
ENST00000324631.13:c.1624C= (CACNB2) MANE Select	ENSP00000320025.8:p.Arg542=
ENST00000377315.5:c.1480C= (CACNB2)	ENSP00000366532.4:p.Arg494=
ENST00000377319.8:c.1345C= (CACNB2)	ENSP00000366536.3:p.Arg449=
ENST00000377329.10:c.1462C= (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Arg488=
ENST00000377331.8:c.1249C= (CACNB2)	ENSP00000366548.4:p.Arg417=
ENST00000643096.2:c.1426C= (CACNB2)	ENSP00000494209.2:p.Arg476=
ENST00000645287.1:c.1468C= (CACNB2)	ENSP00000496203.1:p.Arg490=
ENST00000647168.2:c.*765C= (CACNB2)	ENSP00000495854.2:n.*765C=
ENST00000650685.1:c.1366C= (CACNB2)	ENSP00000498460.1:p.Arg456=
ENST00000651330.1:c.*898C= (CACNB2)	ENSP00000498457.1:n.*898C=
ENST00000651468.1:c.1181C= (CACNB2)	ENSP00000498352.1:n.1181C=
ENST00000651928.1:c.*863C= (CACNB2)	ENSP00000499177.1:n.*863C=
ENST00000652391.1:c.1444C= (CACNB2)	ENSP00000498938.1:p.Arg482=
ENST00000652478.1:c.*724C= (CACNB2)	ENSP00000498812.1:n.*724C=
ENST00000282343.12:c.1540C= (CACNB2)	ENSP00000282343.8:p.Arg514=
ENST00000324631.11:c.1624C= (CACNB2)	ENSP00000320025.7:p.Arg542=
ENST00000352115.10:c.1552C= (CACNB2)	ENSP00000344474.6:p.Arg518=
ENST00000377315.4:c.1480C= (CACNB2)	ENSP00000366532.4:p.Arg494=
ENST00000377319.7:c.1345C= (CACNB2)	ENSP00000366536.3:p.Arg449=
ENST00000377328.5:c.874C= (CACNB2)	ENSP00000366545.1:p.Arg292=
ENST00000377329.8:c.1462C= (CACNB2)	ENSP00000366546.4:p.Arg488=
ENST00000377331.6:c.1468C= (CACNB2)	ENSP00000366548.2:p.Arg490=
ENST00000396576.6:c.1459C= (CACNB2)	ENSP00000379821.2:p.Arg487=
ENST00000612134.4:c.1328C= (CACNB2)	ENSP00000480563.1:n.1328C=
ENST00000612743.1:c.136C= (CACNB2)	ENSP00000478676.1:p.Arg46=
ENST00000615785.4:c.709C= (CACNB2)	ENSP00000480260.1:p.Arg237=
ENST00000617363.4:c.1387C= (CACNB2)	ENSP00000479756.1:p.Arg463=
NM_000724.3:c.1459C= (CACNB2)	NP_000715.2:p.Arg487=
NM_001167945.1:c.1426C= (CACNB2)	NP_001161417.1:p.Arg476=
NM_201570.2:c.1480C= (CACNB2)	NP_963864.1:p.Arg494=
NM_201571.3:c.1540C= (CACNB2)	NP_963865.2:p.Arg514=
NM_201572.3:c.1468C= (CACNB2)	NP_963866.2:p.Arg490=
NM_201590.2:c.1462C= (CACNB2)	NP_963884.2:p.Arg488=
NM_201593.2:c.1510C= (CACNB2)	NP_963887.2:p.Arg504=
NM_201596.2:c.1624C= (CACNB2)	NP_963890.2:p.Arg542=
NM_201597.2:c.1552C= (CACNB2)	NP_963891.1:p.Arg518=
XM_005252588.2:c.1366C= (CACNB2)	XP_005252645.1:p.Arg456=
XM_005252591.2:c.784C= (CACNB2)	XP_005252648.1:p.Arg262=
XM_006717502.2:c.1444C= (CACNB2)	XP_006717565.1:p.Arg482=
XM_011519659.1:c.1390C= (CACNB2)	XP_011517961.1:p.Arg464=
XM_011519660.1:c.1345C= (CACNB2)	XP_011517962.1:p.Arg449=
NM_001330060.1:c.1345C= (CACNB2)	NP_001316989.1:p.Arg449=
XM_005252588.4:c.1366C= (CACNB2)	XP_005252645.1:p.Arg456=
XM_005252591.3:c.784C= (CACNB2)	XP_005252648.1:p.Arg262=
XM_006717502.3:c.1444C= (CACNB2)	XP_006717565.1:p.Arg482=
XM_011519659.2:c.1390C= (CACNB2)	XP_011517961.1:p.Arg464=
XM_017016625.1:c.784C= (CACNB2)	XP_016872114.1:p.Arg262=
XR_001747060.1:n.2423+2704G= (NSUN6)
XR_001747198.1:n.1749C= (CACNB2)
NM_000724.4:c.1459C= (CACNB2)	NP_000715.2:p.Arg487=
NM_001167945.2:c.1426C= (CACNB2)	NP_001161417.1:p.Arg476=
NM_001330060.2:c.1345C= (CACNB2)	NP_001316989.1:p.Arg449=
NM_201570.3:c.1480C= (CACNB2)	NP_963864.1:p.Arg494=
NM_201571.4:c.1540C= (CACNB2)	NP_963865.2:p.Arg514=
NM_201572.4:c.1468C= (CACNB2)	NP_963866.2:p.Arg490=
NM_201590.3:c.1462C= (CACNB2) MANE Plus Clinical	NP_963884.2:p.Arg488=
NM_201593.3:c.1510C= (CACNB2)	NP_963887.2:p.Arg504=
NM_201596.3:c.1624C= (CACNB2) MANE Select	NP_963890.2:p.Arg542=
NM_201597.3:c.1552C= (CACNB2)	NP_963891.1:p.Arg518=