Canonical Allele Identifier: CA2403929692

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564829G= , CM000684.2:g.36564829G=	GRCh38
NC_000022.10:g.36960876G= , CM000684.1:g.36960876G=	GRCh37
NC_000022.9:g.35290822G=	NCBI36
NG_031861.1:g.142815C=
NG_031861.2:g.143030C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.494C= MANE Select	ENSP00000300105.6:p.Ser165=
ENST00000300105.6:c.494C=	ENSP00000300105.6:p.Ser165=
NM_006078.3:c.494C=	NP_006069.1:p.Ser165=
NM_006078.4:c.494C=	NP_006069.1:p.Ser165=
XM_017028531.2:c.236C=	XP_016884020.1:p.Ser79=
NM_001379051.1:c.425C=	NP_001365980.1:p.Ser142=
NM_006078.5:c.494C= MANE Select	NP_006069.1:p.Ser165=
NR_166440.1:n.1860C=