Canonical Allele Identifier: CA376072176

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828448A>C (hg19) ; chr10:g.18539519A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539519A>C , CM000672.2:g.18539519A>C	GRCh38
NC_000010.10:g.18828448A>C , CM000672.1:g.18828448A>C	GRCh37
NC_000010.9:g.18868454A>C	NCBI36
NG_016195.1:g.403843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1634A>C (CACNB2)	ENSP00000366532.4:p.Glu545Ala
ENST00000377319.9:c.1499A>C (CACNB2)	ENSP00000366536.3:p.Glu500Ala
ENST00000645287.2:c.1622A>C (CACNB2)	ENSP00000496203.1:p.Glu541Ala
ENST00000282343.13:c.1694A>C (CACNB2)	ENSP00000282343.8:p.Glu565Ala
ENST00000324631.13:c.1778A>C (CACNB2) MANE Select	ENSP00000320025.8:p.Glu593Ala
ENST00000377315.5:c.1634A>C (CACNB2)	ENSP00000366532.4:p.Glu545Ala
ENST00000377319.8:c.1499A>C (CACNB2)	ENSP00000366536.3:p.Glu500Ala
ENST00000377329.10:c.1616A>C (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Glu539Ala
ENST00000377331.8:c.1403A>C (CACNB2)	ENSP00000366548.4:p.Glu468Ala
ENST00000643096.2:c.1580A>C (CACNB2)	ENSP00000494209.2:p.Glu527Ala
ENST00000645287.1:c.1622A>C (CACNB2)	ENSP00000496203.1:p.Glu541Ala
ENST00000647168.2:c.*919A>C (CACNB2)	ENSP00000495854.2:n.*919A>C
ENST00000650685.1:c.1520A>C (CACNB2)	ENSP00000498460.1:p.Glu507Ala
ENST00000651330.1:c.*1052A>C (CACNB2)	ENSP00000498457.1:n.*1052A>C
ENST00000651468.1:c.1335A>C (CACNB2)	ENSP00000498352.1:n.1335A>C
ENST00000651928.1:c.*1017A>C (CACNB2)	ENSP00000499177.1:n.*1017A>C
ENST00000652391.1:c.1598A>C (CACNB2)	ENSP00000498938.1:p.Glu533Ala
ENST00000652478.1:c.*878A>C (CACNB2)	ENSP00000498812.1:n.*878A>C
ENST00000282343.12:c.1694A>C (CACNB2)	ENSP00000282343.8:p.Glu565Ala
ENST00000324631.11:c.1778A>C (CACNB2)	ENSP00000320025.7:p.Glu593Ala
ENST00000352115.10:c.1706A>C (CACNB2)	ENSP00000344474.6:p.Glu569Ala
ENST00000377315.4:c.1634A>C (CACNB2)	ENSP00000366532.4:p.Glu545Ala
ENST00000377319.7:c.1499A>C (CACNB2)	ENSP00000366536.3:p.Glu500Ala
ENST00000377328.5:c.1028A>C (CACNB2)	ENSP00000366545.1:p.Glu343Ala
ENST00000377329.8:c.1616A>C (CACNB2)	ENSP00000366546.4:p.Glu539Ala
ENST00000377331.6:c.1622A>C (CACNB2)	ENSP00000366548.2:p.Glu541Ala
ENST00000396576.6:c.1613A>C (CACNB2)	ENSP00000379821.2:p.Glu538Ala
ENST00000612134.4:c.1482A>C (CACNB2)	ENSP00000480563.1:n.1482A>C
ENST00000612743.1:c.290A>C (CACNB2)	ENSP00000478676.1:p.Glu97Ala
ENST00000615785.4:c.863A>C (CACNB2)	ENSP00000480260.1:p.Glu288Ala
ENST00000617363.4:c.1541A>C (CACNB2)	ENSP00000479756.1:p.Glu514Ala
NM_000724.3:c.1613A>C (CACNB2)	NP_000715.2:p.Glu538Ala
NM_001167945.1:c.1580A>C (CACNB2)	NP_001161417.1:p.Glu527Ala
NM_201570.2:c.1634A>C (CACNB2)	NP_963864.1:p.Glu545Ala
NM_201571.3:c.1694A>C (CACNB2)	NP_963865.2:p.Glu565Ala
NM_201572.3:c.1622A>C (CACNB2)	NP_963866.2:p.Glu541Ala
NM_201590.2:c.1616A>C (CACNB2)	NP_963884.2:p.Glu539Ala
NM_201593.2:c.1664A>C (CACNB2)	NP_963887.2:p.Glu555Ala
NM_201596.2:c.1778A>C (CACNB2)	NP_963890.2:p.Glu593Ala
NM_201597.2:c.1706A>C (CACNB2)	NP_963891.1:p.Glu569Ala
XM_005252588.2:c.1520A>C (CACNB2)	XP_005252645.1:p.Glu507Ala
XM_005252591.2:c.938A>C (CACNB2)	XP_005252648.1:p.Glu313Ala
XM_006717502.2:c.1598A>C (CACNB2)	XP_006717565.1:p.Glu533Ala
XM_011519659.1:c.1544A>C (CACNB2)	XP_011517961.1:p.Glu515Ala
XM_011519660.1:c.1499A>C (CACNB2)	XP_011517962.1:p.Glu500Ala
NM_001330060.1:c.1499A>C (CACNB2)	NP_001316989.1:p.Glu500Ala
XM_005252588.4:c.1520A>C (CACNB2)	XP_005252645.1:p.Glu507Ala
XM_005252591.3:c.938A>C (CACNB2)	XP_005252648.1:p.Glu313Ala
XM_006717502.3:c.1598A>C (CACNB2)	XP_006717565.1:p.Glu533Ala
XM_011519659.2:c.1544A>C (CACNB2)	XP_011517961.1:p.Glu515Ala
XM_017016625.1:c.938A>C (CACNB2)	XP_016872114.1:p.Glu313Ala
XR_001747060.1:n.2423+2550T>G (NSUN6)
XR_001747198.1:n.1903A>C (CACNB2)
NM_000724.4:c.1613A>C (CACNB2)	NP_000715.2:p.Glu538Ala
NM_001167945.2:c.1580A>C (CACNB2)	NP_001161417.1:p.Glu527Ala
NM_001330060.2:c.1499A>C (CACNB2)	NP_001316989.1:p.Glu500Ala
NM_201570.3:c.1634A>C (CACNB2)	NP_963864.1:p.Glu545Ala
NM_201571.4:c.1694A>C (CACNB2)	NP_963865.2:p.Glu565Ala
NM_201572.4:c.1622A>C (CACNB2)	NP_963866.2:p.Glu541Ala
NM_201590.3:c.1616A>C (CACNB2) MANE Plus Clinical	NP_963884.2:p.Glu539Ala
NM_201593.3:c.1664A>C (CACNB2)	NP_963887.2:p.Glu555Ala
NM_201596.3:c.1778A>C (CACNB2) MANE Select	NP_963890.2:p.Glu593Ala
NM_201597.3:c.1706A>C (CACNB2)	NP_963891.1:p.Glu569Ala