Canonical Allele Identifier: CA1436421929

Gene: SORCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.7532876A= , CM000666.2:g.7532876A=	GRCh38
NC_000004.11:g.7534603A= , CM000666.1:g.7534603A=	GRCh37
NC_000004.10:g.7585503A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329016.10:c.132+1247A=	ENSP00000329124.10:n.132+1247A=
ENST00000507866.6:c.648+1247A= MANE Select	ENSP00000422185.2:n.648+1247A=
ENST00000511199.1:n.263+1247A=
NM_020777.2:c.648+1247A=	NP_065828.2:n.648+1247A=
XM_005247987.3:c.648+1247A=	XP_005248044.2:n.648+1247A=
XM_011513514.1:c.648+1247A=	XP_011511816.1:n.648+1247A=
XM_011513515.1:c.648+1247A=	XP_011511817.1:n.648+1247A=
XM_011513516.1:c.648+1247A=	XP_011511818.1:n.648+1247A=
XM_011513517.1:c.255+1247A=	XP_011511819.1:n.255+1247A=
XM_005247987.4:c.648+1247A=	XP_005248044.2:n.648+1247A=
XM_011513514.2:c.648+1247A=	XP_011511816.1:n.648+1247A=
XM_011513515.2:c.648+1247A=	XP_011511817.1:n.648+1247A=
XM_011513516.2:c.648+1247A=	XP_011511818.1:n.648+1247A=
XM_017008481.1:c.648+1247A=	XP_016863970.1:n.648+1247A=
NM_020777.3:c.648+1247A= MANE Select	NP_065828.2:n.648+1247A=