Canonical Allele Identifier: CA376072298

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828467C>A (hg19) ; chr10:g.18539538C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539538C>A , CM000672.2:g.18539538C>A	GRCh38
NC_000010.10:g.18828467C>A , CM000672.1:g.18828467C>A	GRCh37
NC_000010.9:g.18868473C>A	NCBI36
NG_016195.1:g.403862C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1653C>A (CACNB2)	ENSP00000366532.4:p.Asp551Glu
ENST00000377319.9:c.1518C>A (CACNB2)	ENSP00000366536.3:p.Asp506Glu
ENST00000645287.2:c.1641C>A (CACNB2)	ENSP00000496203.1:p.Asp547Glu
ENST00000282343.13:c.1713C>A (CACNB2)	ENSP00000282343.8:p.Asp571Glu
ENST00000324631.13:c.1797C>A (CACNB2) MANE Select	ENSP00000320025.8:p.Asp599Glu
ENST00000377315.5:c.1653C>A (CACNB2)	ENSP00000366532.4:p.Asp551Glu
ENST00000377319.8:c.1518C>A (CACNB2)	ENSP00000366536.3:p.Asp506Glu
ENST00000377329.10:c.1635C>A (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Asp545Glu
ENST00000377331.8:c.1422C>A (CACNB2)	ENSP00000366548.4:p.Asp474Glu
ENST00000643096.2:c.1599C>A (CACNB2)	ENSP00000494209.2:p.Asp533Glu
ENST00000645287.1:c.1641C>A (CACNB2)	ENSP00000496203.1:p.Asp547Glu
ENST00000647168.2:c.*938C>A (CACNB2)	ENSP00000495854.2:n.*938C>A
ENST00000650685.1:c.1539C>A (CACNB2)	ENSP00000498460.1:p.Asp513Glu
ENST00000651330.1:c.*1071C>A (CACNB2)	ENSP00000498457.1:n.*1071C>A
ENST00000651468.1:c.1354C>A (CACNB2)	ENSP00000498352.1:n.1354C>A
ENST00000651928.1:c.*1036C>A (CACNB2)	ENSP00000499177.1:n.*1036C>A
ENST00000652391.1:c.1617C>A (CACNB2)	ENSP00000498938.1:p.Asp539Glu
ENST00000652478.1:c.*897C>A (CACNB2)	ENSP00000498812.1:n.*897C>A
ENST00000282343.12:c.1713C>A (CACNB2)	ENSP00000282343.8:p.Asp571Glu
ENST00000324631.11:c.1797C>A (CACNB2)	ENSP00000320025.7:p.Asp599Glu
ENST00000352115.10:c.1725C>A (CACNB2)	ENSP00000344474.6:p.Asp575Glu
ENST00000377315.4:c.1653C>A (CACNB2)	ENSP00000366532.4:p.Asp551Glu
ENST00000377319.7:c.1518C>A (CACNB2)	ENSP00000366536.3:p.Asp506Glu
ENST00000377328.5:c.1047C>A (CACNB2)	ENSP00000366545.1:p.Asp349Glu
ENST00000377329.8:c.1635C>A (CACNB2)	ENSP00000366546.4:p.Asp545Glu
ENST00000377331.6:c.1641C>A (CACNB2)	ENSP00000366548.2:p.Asp547Glu
ENST00000396576.6:c.1632C>A (CACNB2)	ENSP00000379821.2:p.Asp544Glu
ENST00000612134.4:c.1501C>A (CACNB2)	ENSP00000480563.1:n.1501C>A
ENST00000612743.1:c.309C>A (CACNB2)	ENSP00000478676.1:p.Asp103Glu
ENST00000615785.4:c.882C>A (CACNB2)	ENSP00000480260.1:p.Asp294Glu
ENST00000617363.4:c.1560C>A (CACNB2)	ENSP00000479756.1:p.Asp520Glu
NM_000724.3:c.1632C>A (CACNB2)	NP_000715.2:p.Asp544Glu
NM_001167945.1:c.1599C>A (CACNB2)	NP_001161417.1:p.Asp533Glu
NM_201570.2:c.1653C>A (CACNB2)	NP_963864.1:p.Asp551Glu
NM_201571.3:c.1713C>A (CACNB2)	NP_963865.2:p.Asp571Glu
NM_201572.3:c.1641C>A (CACNB2)	NP_963866.2:p.Asp547Glu
NM_201590.2:c.1635C>A (CACNB2)	NP_963884.2:p.Asp545Glu
NM_201593.2:c.1683C>A (CACNB2)	NP_963887.2:p.Asp561Glu
NM_201596.2:c.1797C>A (CACNB2)	NP_963890.2:p.Asp599Glu
NM_201597.2:c.1725C>A (CACNB2)	NP_963891.1:p.Asp575Glu
XM_005252588.2:c.1539C>A (CACNB2)	XP_005252645.1:p.Asp513Glu
XM_005252591.2:c.957C>A (CACNB2)	XP_005252648.1:p.Asp319Glu
XM_006717502.2:c.1617C>A (CACNB2)	XP_006717565.1:p.Asp539Glu
XM_011519659.1:c.1563C>A (CACNB2)	XP_011517961.1:p.Asp521Glu
XM_011519660.1:c.1518C>A (CACNB2)	XP_011517962.1:p.Asp506Glu
NM_001330060.1:c.1518C>A (CACNB2)	NP_001316989.1:p.Asp506Glu
XM_005252588.4:c.1539C>A (CACNB2)	XP_005252645.1:p.Asp513Glu
XM_005252591.3:c.957C>A (CACNB2)	XP_005252648.1:p.Asp319Glu
XM_006717502.3:c.1617C>A (CACNB2)	XP_006717565.1:p.Asp539Glu
XM_011519659.2:c.1563C>A (CACNB2)	XP_011517961.1:p.Asp521Glu
XM_017016625.1:c.957C>A (CACNB2)	XP_016872114.1:p.Asp319Glu
XR_001747060.1:n.2423+2531G>T (NSUN6)
XR_001747198.1:n.1922C>A (CACNB2)
NM_000724.4:c.1632C>A (CACNB2)	NP_000715.2:p.Asp544Glu
NM_001167945.2:c.1599C>A (CACNB2)	NP_001161417.1:p.Asp533Glu
NM_001330060.2:c.1518C>A (CACNB2)	NP_001316989.1:p.Asp506Glu
NM_201570.3:c.1653C>A (CACNB2)	NP_963864.1:p.Asp551Glu
NM_201571.4:c.1713C>A (CACNB2)	NP_963865.2:p.Asp571Glu
NM_201572.4:c.1641C>A (CACNB2)	NP_963866.2:p.Asp547Glu
NM_201590.3:c.1635C>A (CACNB2) MANE Plus Clinical	NP_963884.2:p.Asp545Glu
NM_201593.3:c.1683C>A (CACNB2)	NP_963887.2:p.Asp561Glu
NM_201596.3:c.1797C>A (CACNB2) MANE Select	NP_963890.2:p.Asp599Glu
NM_201597.3:c.1725C>A (CACNB2)	NP_963891.1:p.Asp575Glu