Canonical Allele Identifier: CA1894173436

Gene: CACNB2 NSUN6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539455G= , CM000672.2:g.18539455G=	GRCh38
NC_000010.10:g.18828384G= , CM000672.1:g.18828384G=	GRCh37
NC_000010.9:g.18868390G=	NCBI36
NG_016195.1:g.403779G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1570G= (CACNB2)	ENSP00000366532.4:p.Glu524=
ENST00000377319.9:c.1435G= (CACNB2)	ENSP00000366536.3:p.Glu479=
ENST00000645287.2:c.1558G= (CACNB2)	ENSP00000496203.1:p.Glu520=
ENST00000282343.13:c.1630G= (CACNB2)	ENSP00000282343.8:p.Glu544=
ENST00000324631.13:c.1714G= (CACNB2) MANE Select	ENSP00000320025.8:p.Glu572=
ENST00000377315.5:c.1570G= (CACNB2)	ENSP00000366532.4:p.Glu524=
ENST00000377319.8:c.1435G= (CACNB2)	ENSP00000366536.3:p.Glu479=
ENST00000377329.10:c.1552G= (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Glu518=
ENST00000377331.8:c.1339G= (CACNB2)	ENSP00000366548.4:p.Glu447=
ENST00000643096.2:c.1516G= (CACNB2)	ENSP00000494209.2:p.Glu506=
ENST00000645287.1:c.1558G= (CACNB2)	ENSP00000496203.1:p.Glu520=
ENST00000647168.2:c.*855G= (CACNB2)	ENSP00000495854.2:n.*855G=
ENST00000650685.1:c.1456G= (CACNB2)	ENSP00000498460.1:p.Glu486=
ENST00000651330.1:c.*988G= (CACNB2)	ENSP00000498457.1:n.*988G=
ENST00000651468.1:c.1271G= (CACNB2)	ENSP00000498352.1:n.1271G=
ENST00000651928.1:c.*953G= (CACNB2)	ENSP00000499177.1:n.*953G=
ENST00000652391.1:c.1534G= (CACNB2)	ENSP00000498938.1:p.Glu512=
ENST00000652478.1:c.*814G= (CACNB2)	ENSP00000498812.1:n.*814G=
ENST00000282343.12:c.1630G= (CACNB2)	ENSP00000282343.8:p.Glu544=
ENST00000324631.11:c.1714G= (CACNB2)	ENSP00000320025.7:p.Glu572=
ENST00000352115.10:c.1642G= (CACNB2)	ENSP00000344474.6:p.Glu548=
ENST00000377315.4:c.1570G= (CACNB2)	ENSP00000366532.4:p.Glu524=
ENST00000377319.7:c.1435G= (CACNB2)	ENSP00000366536.3:p.Glu479=
ENST00000377328.5:c.964G= (CACNB2)	ENSP00000366545.1:p.Glu322=
ENST00000377329.8:c.1552G= (CACNB2)	ENSP00000366546.4:p.Glu518=
ENST00000377331.6:c.1558G= (CACNB2)	ENSP00000366548.2:p.Glu520=
ENST00000396576.6:c.1549G= (CACNB2)	ENSP00000379821.2:p.Glu517=
ENST00000612134.4:c.1418G= (CACNB2)	ENSP00000480563.1:n.1418G=
ENST00000612743.1:c.226G= (CACNB2)	ENSP00000478676.1:p.Glu76=
ENST00000615785.4:c.799G= (CACNB2)	ENSP00000480260.1:p.Glu267=
ENST00000617363.4:c.1477G= (CACNB2)	ENSP00000479756.1:p.Glu493=
NM_000724.3:c.1549G= (CACNB2)	NP_000715.2:p.Glu517=
NM_001167945.1:c.1516G= (CACNB2)	NP_001161417.1:p.Glu506=
NM_201570.2:c.1570G= (CACNB2)	NP_963864.1:p.Glu524=
NM_201571.3:c.1630G= (CACNB2)	NP_963865.2:p.Glu544=
NM_201572.3:c.1558G= (CACNB2)	NP_963866.2:p.Glu520=
NM_201590.2:c.1552G= (CACNB2)	NP_963884.2:p.Glu518=
NM_201593.2:c.1600G= (CACNB2)	NP_963887.2:p.Glu534=
NM_201596.2:c.1714G= (CACNB2)	NP_963890.2:p.Glu572=
NM_201597.2:c.1642G= (CACNB2)	NP_963891.1:p.Glu548=
XM_005252588.2:c.1456G= (CACNB2)	XP_005252645.1:p.Glu486=
XM_005252591.2:c.874G= (CACNB2)	XP_005252648.1:p.Glu292=
XM_006717502.2:c.1534G= (CACNB2)	XP_006717565.1:p.Glu512=
XM_011519659.1:c.1480G= (CACNB2)	XP_011517961.1:p.Glu494=
XM_011519660.1:c.1435G= (CACNB2)	XP_011517962.1:p.Glu479=
NM_001330060.1:c.1435G= (CACNB2)	NP_001316989.1:p.Glu479=
XM_005252588.4:c.1456G= (CACNB2)	XP_005252645.1:p.Glu486=
XM_005252591.3:c.874G= (CACNB2)	XP_005252648.1:p.Glu292=
XM_006717502.3:c.1534G= (CACNB2)	XP_006717565.1:p.Glu512=
XM_011519659.2:c.1480G= (CACNB2)	XP_011517961.1:p.Glu494=
XM_017016625.1:c.874G= (CACNB2)	XP_016872114.1:p.Glu292=
XR_001747060.1:n.2423+2614C= (NSUN6)
XR_001747198.1:n.1839G= (CACNB2)
NM_000724.4:c.1549G= (CACNB2)	NP_000715.2:p.Glu517=
NM_001167945.2:c.1516G= (CACNB2)	NP_001161417.1:p.Glu506=
NM_001330060.2:c.1435G= (CACNB2)	NP_001316989.1:p.Glu479=
NM_201570.3:c.1570G= (CACNB2)	NP_963864.1:p.Glu524=
NM_201571.4:c.1630G= (CACNB2)	NP_963865.2:p.Glu544=
NM_201572.4:c.1558G= (CACNB2)	NP_963866.2:p.Glu520=
NM_201590.3:c.1552G= (CACNB2) MANE Plus Clinical	NP_963884.2:p.Glu518=
NM_201593.3:c.1600G= (CACNB2)	NP_963887.2:p.Glu534=
NM_201596.3:c.1714G= (CACNB2) MANE Select	NP_963890.2:p.Glu572=
NM_201597.3:c.1642G= (CACNB2)	NP_963891.1:p.Glu548=