Canonical Allele Identifier: CA1436358594

Gene: SORCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.7422024C= , CM000666.2:g.7422024C=	GRCh38
NC_000004.11:g.7423751C= , CM000666.1:g.7423751C=	GRCh37
NC_000004.10:g.7474652C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020777.3:c.548+25669C= MANE Select	NP_065828.2:n.548+25669C=
ENST00000507866.6:c.548+25669C= MANE Select	ENSP00000422185.2:n.548+25669C=
NM_020777.2:c.548+25669C=	NP_065828.2:n.548+25669C=
ENST00000329016.10:c.32+25669C=	ENSP00000329124.10:n.32+25669C=
ENST00000511199.1:n.163+25669C=
XM_005247987.3:c.548+25669C=	XP_005248044.2:n.548+25669C=
XM_005247987.4:c.548+25669C=	XP_005248044.2:n.548+25669C=
XM_011513514.1:c.548+25669C=	XP_011511816.1:n.548+25669C=
XM_011513514.2:c.548+25669C=	XP_011511816.1:n.548+25669C=
XM_011513515.1:c.548+25669C=	XP_011511817.1:n.548+25669C=
XM_011513515.2:c.548+25669C=	XP_011511817.1:n.548+25669C=
XM_011513516.1:c.548+25669C=	XP_011511818.1:n.548+25669C=
XM_011513516.2:c.548+25669C=	XP_011511818.1:n.548+25669C=
XM_011513517.1:c.155+25669C=	XP_011511819.1:n.155+25669C=
XM_017008481.1:c.548+25669C=	XP_016863970.1:n.548+25669C=