Canonical Allele Identifier: CA376071864

Gene: CACNB2 NSUN6

Linked Data

• dbSNP Id: rs1554842932
• MyVariant Identifiers: chr10:g.18828381A>T (hg19) ; chr10:g.18539452A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539452A>T , CM000672.2:g.18539452A>T	GRCh38
NC_000010.10:g.18828381A>T , CM000672.1:g.18828381A>T	GRCh37
NC_000010.9:g.18868387A>T	NCBI36
NG_016195.1:g.403776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1567A>T (CACNB2)	ENSP00000366532.4:p.Lys523Ter
ENST00000377319.9:c.1432A>T (CACNB2)	ENSP00000366536.3:p.Lys478Ter
ENST00000645287.2:c.1555A>T (CACNB2)	ENSP00000496203.1:p.Lys519Ter
ENST00000282343.13:c.1627A>T (CACNB2)	ENSP00000282343.8:p.Lys543Ter
ENST00000324631.13:c.1711A>T (CACNB2) MANE Select	ENSP00000320025.8:p.Lys571Ter
ENST00000377315.5:c.1567A>T (CACNB2)	ENSP00000366532.4:p.Lys523Ter
ENST00000377319.8:c.1432A>T (CACNB2)	ENSP00000366536.3:p.Lys478Ter
ENST00000377329.10:c.1549A>T (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Lys517Ter
ENST00000377331.8:c.1336A>T (CACNB2)	ENSP00000366548.4:p.Lys446Ter
ENST00000643096.2:c.1513A>T (CACNB2)	ENSP00000494209.2:p.Lys505Ter
ENST00000645287.1:c.1555A>T (CACNB2)	ENSP00000496203.1:p.Lys519Ter
ENST00000647168.2:c.*852A>T (CACNB2)	ENSP00000495854.2:n.*852A>T
ENST00000650685.1:c.1453A>T (CACNB2)	ENSP00000498460.1:p.Lys485Ter
ENST00000651330.1:c.*985A>T (CACNB2)	ENSP00000498457.1:n.*985A>T
ENST00000651468.1:c.1268A>T (CACNB2)	ENSP00000498352.1:n.1268A>T
ENST00000651928.1:c.*950A>T (CACNB2)	ENSP00000499177.1:n.*950A>T
ENST00000652391.1:c.1531A>T (CACNB2)	ENSP00000498938.1:p.Lys511Ter
ENST00000652478.1:c.*811A>T (CACNB2)	ENSP00000498812.1:n.*811A>T
ENST00000282343.12:c.1627A>T (CACNB2)	ENSP00000282343.8:p.Lys543Ter
ENST00000324631.11:c.1711A>T (CACNB2)	ENSP00000320025.7:p.Lys571Ter
ENST00000352115.10:c.1639A>T (CACNB2)	ENSP00000344474.6:p.Lys547Ter
ENST00000377315.4:c.1567A>T (CACNB2)	ENSP00000366532.4:p.Lys523Ter
ENST00000377319.7:c.1432A>T (CACNB2)	ENSP00000366536.3:p.Lys478Ter
ENST00000377328.5:c.961A>T (CACNB2)	ENSP00000366545.1:p.Lys321Ter
ENST00000377329.8:c.1549A>T (CACNB2)	ENSP00000366546.4:p.Lys517Ter
ENST00000377331.6:c.1555A>T (CACNB2)	ENSP00000366548.2:p.Lys519Ter
ENST00000396576.6:c.1546A>T (CACNB2)	ENSP00000379821.2:p.Lys516Ter
ENST00000612134.4:c.1415A>T (CACNB2)	ENSP00000480563.1:n.1415A>T
ENST00000612743.1:c.223A>T (CACNB2)	ENSP00000478676.1:p.Lys75Ter
ENST00000615785.4:c.796A>T (CACNB2)	ENSP00000480260.1:p.Lys266Ter
ENST00000617363.4:c.1474A>T (CACNB2)	ENSP00000479756.1:p.Lys492Ter
NM_000724.3:c.1546A>T (CACNB2)	NP_000715.2:p.Lys516Ter
NM_001167945.1:c.1513A>T (CACNB2)	NP_001161417.1:p.Lys505Ter
NM_201570.2:c.1567A>T (CACNB2)	NP_963864.1:p.Lys523Ter
NM_201571.3:c.1627A>T (CACNB2)	NP_963865.2:p.Lys543Ter
NM_201572.3:c.1555A>T (CACNB2)	NP_963866.2:p.Lys519Ter
NM_201590.2:c.1549A>T (CACNB2)	NP_963884.2:p.Lys517Ter
NM_201593.2:c.1597A>T (CACNB2)	NP_963887.2:p.Lys533Ter
NM_201596.2:c.1711A>T (CACNB2)	NP_963890.2:p.Lys571Ter
NM_201597.2:c.1639A>T (CACNB2)	NP_963891.1:p.Lys547Ter
XM_005252588.2:c.1453A>T (CACNB2)	XP_005252645.1:p.Lys485Ter
XM_005252591.2:c.871A>T (CACNB2)	XP_005252648.1:p.Lys291Ter
XM_006717502.2:c.1531A>T (CACNB2)	XP_006717565.1:p.Lys511Ter
XM_011519659.1:c.1477A>T (CACNB2)	XP_011517961.1:p.Lys493Ter
XM_011519660.1:c.1432A>T (CACNB2)	XP_011517962.1:p.Lys478Ter
NM_001330060.1:c.1432A>T (CACNB2)	NP_001316989.1:p.Lys478Ter
XM_005252588.4:c.1453A>T (CACNB2)	XP_005252645.1:p.Lys485Ter
XM_005252591.3:c.871A>T (CACNB2)	XP_005252648.1:p.Lys291Ter
XM_006717502.3:c.1531A>T (CACNB2)	XP_006717565.1:p.Lys511Ter
XM_011519659.2:c.1477A>T (CACNB2)	XP_011517961.1:p.Lys493Ter
XM_017016625.1:c.871A>T (CACNB2)	XP_016872114.1:p.Lys291Ter
XR_001747060.1:n.2423+2617T>A (NSUN6)
XR_001747198.1:n.1836A>T (CACNB2)
NM_000724.4:c.1546A>T (CACNB2)	NP_000715.2:p.Lys516Ter
NM_001167945.2:c.1513A>T (CACNB2)	NP_001161417.1:p.Lys505Ter
NM_001330060.2:c.1432A>T (CACNB2)	NP_001316989.1:p.Lys478Ter
NM_201570.3:c.1567A>T (CACNB2)	NP_963864.1:p.Lys523Ter
NM_201571.4:c.1627A>T (CACNB2)	NP_963865.2:p.Lys543Ter
NM_201572.4:c.1555A>T (CACNB2)	NP_963866.2:p.Lys519Ter
NM_201590.3:c.1549A>T (CACNB2) MANE Plus Clinical	NP_963884.2:p.Lys517Ter
NM_201593.3:c.1597A>T (CACNB2)	NP_963887.2:p.Lys533Ter
NM_201596.3:c.1711A>T (CACNB2) MANE Select	NP_963890.2:p.Lys571Ter
NM_201597.3:c.1639A>T (CACNB2)	NP_963891.1:p.Lys547Ter