Canonical Allele Identifier: CA1894173249

Gene: CACNB2 NSUN6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539380C= , CM000672.2:g.18539380C=	GRCh38
NC_000010.10:g.18828309C= , CM000672.1:g.18828309C=	GRCh37
NC_000010.9:g.18868315C=	NCBI36
NG_016195.1:g.403704C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1495C= (CACNB2)	ENSP00000366532.4:p.Arg499=
ENST00000377319.9:c.1360C= (CACNB2)	ENSP00000366536.3:p.Arg454=
ENST00000645287.2:c.1483C= (CACNB2)	ENSP00000496203.1:p.Arg495=
ENST00000282343.13:c.1555C= (CACNB2)	ENSP00000282343.8:p.Arg519=
ENST00000324631.13:c.1639C= (CACNB2) MANE Select	ENSP00000320025.8:p.Arg547=
ENST00000377315.5:c.1495C= (CACNB2)	ENSP00000366532.4:p.Arg499=
ENST00000377319.8:c.1360C= (CACNB2)	ENSP00000366536.3:p.Arg454=
ENST00000377329.10:c.1477C= (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Arg493=
ENST00000377331.8:c.1264C= (CACNB2)	ENSP00000366548.4:p.Arg422=
ENST00000643096.2:c.1441C= (CACNB2)	ENSP00000494209.2:p.Arg481=
ENST00000645287.1:c.1483C= (CACNB2)	ENSP00000496203.1:p.Arg495=
ENST00000647168.2:c.*780C= (CACNB2)	ENSP00000495854.2:n.*780C=
ENST00000650685.1:c.1381C= (CACNB2)	ENSP00000498460.1:p.Arg461=
ENST00000651330.1:c.*913C= (CACNB2)	ENSP00000498457.1:n.*913C=
ENST00000651468.1:c.1196C= (CACNB2)	ENSP00000498352.1:n.1196C=
ENST00000651928.1:c.*878C= (CACNB2)	ENSP00000499177.1:n.*878C=
ENST00000652391.1:c.1459C= (CACNB2)	ENSP00000498938.1:p.Arg487=
ENST00000652478.1:c.*739C= (CACNB2)	ENSP00000498812.1:n.*739C=
ENST00000282343.12:c.1555C= (CACNB2)	ENSP00000282343.8:p.Arg519=
ENST00000324631.11:c.1639C= (CACNB2)	ENSP00000320025.7:p.Arg547=
ENST00000352115.10:c.1567C= (CACNB2)	ENSP00000344474.6:p.Arg523=
ENST00000377315.4:c.1495C= (CACNB2)	ENSP00000366532.4:p.Arg499=
ENST00000377319.7:c.1360C= (CACNB2)	ENSP00000366536.3:p.Arg454=
ENST00000377328.5:c.889C= (CACNB2)	ENSP00000366545.1:p.Arg297=
ENST00000377329.8:c.1477C= (CACNB2)	ENSP00000366546.4:p.Arg493=
ENST00000377331.6:c.1483C= (CACNB2)	ENSP00000366548.2:p.Arg495=
ENST00000396576.6:c.1474C= (CACNB2)	ENSP00000379821.2:p.Arg492=
ENST00000612134.4:c.1343C= (CACNB2)	ENSP00000480563.1:n.1343C=
ENST00000612743.1:c.151C= (CACNB2)	ENSP00000478676.1:p.Arg51=
ENST00000615785.4:c.724C= (CACNB2)	ENSP00000480260.1:p.Arg242=
ENST00000617363.4:c.1402C= (CACNB2)	ENSP00000479756.1:p.Arg468=
NM_000724.3:c.1474C= (CACNB2)	NP_000715.2:p.Arg492=
NM_001167945.1:c.1441C= (CACNB2)	NP_001161417.1:p.Arg481=
NM_201570.2:c.1495C= (CACNB2)	NP_963864.1:p.Arg499=
NM_201571.3:c.1555C= (CACNB2)	NP_963865.2:p.Arg519=
NM_201572.3:c.1483C= (CACNB2)	NP_963866.2:p.Arg495=
NM_201590.2:c.1477C= (CACNB2)	NP_963884.2:p.Arg493=
NM_201593.2:c.1525C= (CACNB2)	NP_963887.2:p.Arg509=
NM_201596.2:c.1639C= (CACNB2)	NP_963890.2:p.Arg547=
NM_201597.2:c.1567C= (CACNB2)	NP_963891.1:p.Arg523=
XM_005252588.2:c.1381C= (CACNB2)	XP_005252645.1:p.Arg461=
XM_005252591.2:c.799C= (CACNB2)	XP_005252648.1:p.Arg267=
XM_006717502.2:c.1459C= (CACNB2)	XP_006717565.1:p.Arg487=
XM_011519659.1:c.1405C= (CACNB2)	XP_011517961.1:p.Arg469=
XM_011519660.1:c.1360C= (CACNB2)	XP_011517962.1:p.Arg454=
NM_001330060.1:c.1360C= (CACNB2)	NP_001316989.1:p.Arg454=
XM_005252588.4:c.1381C= (CACNB2)	XP_005252645.1:p.Arg461=
XM_005252591.3:c.799C= (CACNB2)	XP_005252648.1:p.Arg267=
XM_006717502.3:c.1459C= (CACNB2)	XP_006717565.1:p.Arg487=
XM_011519659.2:c.1405C= (CACNB2)	XP_011517961.1:p.Arg469=
XM_017016625.1:c.799C= (CACNB2)	XP_016872114.1:p.Arg267=
XR_001747060.1:n.2423+2689G= (NSUN6)
XR_001747198.1:n.1764C= (CACNB2)
NM_000724.4:c.1474C= (CACNB2)	NP_000715.2:p.Arg492=
NM_001167945.2:c.1441C= (CACNB2)	NP_001161417.1:p.Arg481=
NM_001330060.2:c.1360C= (CACNB2)	NP_001316989.1:p.Arg454=
NM_201570.3:c.1495C= (CACNB2)	NP_963864.1:p.Arg499=
NM_201571.4:c.1555C= (CACNB2)	NP_963865.2:p.Arg519=
NM_201572.4:c.1483C= (CACNB2)	NP_963866.2:p.Arg495=
NM_201590.3:c.1477C= (CACNB2) MANE Plus Clinical	NP_963884.2:p.Arg493=
NM_201593.3:c.1525C= (CACNB2)	NP_963887.2:p.Arg509=
NM_201596.3:c.1639C= (CACNB2) MANE Select	NP_963890.2:p.Arg547=
NM_201597.3:c.1567C= (CACNB2)	NP_963891.1:p.Arg523=