Canonical Allele Identifier: CA1556433711

Gene: SV2C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76143456A= , CM000667.2:g.76143456A=	GRCh38
NC_000005.9:g.75439281A= , CM000667.1:g.75439281A=	GRCh37
NC_000005.8:g.75475037A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502798.7:c.580+11126A= MANE Select	ENSP00000423541.2:n.580+11126A=
ENST00000322285.7:c.580+11126A=	ENSP00000316983.7:n.580+11126A=
ENST00000502798.6:c.580+11126A=	ENSP00000423541.2:n.580+11126A=
NM_001297716.1:c.580+11126A=	NP_001284645.1:n.580+11126A=
NM_014979.3:c.580+11126A=	NP_055794.3:n.580+11126A=
XM_011543281.1:c.580+11126A=	XP_011541583.1:n.580+11126A=
XM_011543282.1:c.8+11126A=	XP_011541584.1:n.8+11126A=
XM_011543281.3:c.580+11126A=	XP_011541583.1:n.580+11126A=
XM_011543282.3:c.580+11126A=	XP_011541584.2:n.580+11126A=
NM_014979.4:c.580+11126A= MANE Select	NP_055794.3:n.580+11126A=
NM_001297716.2:c.580+11126A=	NP_001284645.1:n.580+11126A=