Canonical Allele Identifier: CA2004929226

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121618736A= , CM000673.2:g.121618736A=	GRCh38
NC_000011.9:g.121489445A= , CM000673.1:g.121489445A=	GRCh37
NC_000011.8:g.120994655A=	NCBI36
NG_023313.1:g.171485A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.5605-38A= MANE Select	ENSP00000260197.6:n.5605-38A=
ENST00000260197.11:c.5605-38A=	ENSP00000260197.6:n.5605-38A=
ENST00000524633.1:n.771-38A=
ENST00000525532.5:c.2437-38A=	ENSP00000434634.1:n.2437-38A=
ENST00000527934.1:c.1450-38A=	ENSP00000435405.1:n.1450-38A=
ENST00000528339.5:n.3242-38A=
ENST00000532694.5:c.2143-38A=	ENSP00000432131.1:n.2143-38A=
ENST00000534286.5:c.2335-38A=	ENSP00000436447.1:n.2335-38A=
ENST00000534754.5:n.1767-38A=
NM_003105.5:c.5605-38A=	NP_003096.1:n.5605-38A=
XM_011542963.1:c.5491-38A=	XP_011541265.1:n.5491-38A=
XM_011542965.1:c.4066-38A=	XP_011541267.1:n.4066-38A=
XM_011542966.1:c.2965-38A=	XP_011541268.1:n.2965-38A=
XM_011542967.1:c.2437-38A=	XP_011541269.1:n.2437-38A=
XM_011542963.3:c.5491-38A=	XP_011541265.1:n.5491-38A=
XM_011542965.3:c.4066-38A=	XP_011541267.1:n.4066-38A=
XM_011542967.3:c.2437-38A=	XP_011541269.1:n.2437-38A=
XM_017018169.2:c.5293-38A=	XP_016873658.1:n.5293-38A=
XM_017018170.2:c.5080-38A=	XP_016873659.1:n.5080-38A=
XM_017018172.2:c.2965-38A=	XP_016873661.1:n.2965-38A=
NM_003105.6:c.5605-38A= MANE Select	NP_003096.2:n.5605-38A=