Canonical Allele Identifier: CA2004922112

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605125T= , CM000673.2:g.121605125T=	GRCh38
NC_000011.9:g.121475834T= , CM000673.1:g.121475834T=	GRCh37
NC_000011.8:g.120981044T=	NCBI36
NG_023313.1:g.157874T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4664T= MANE Select	ENSP00000260197.6:p.Val1555=
ENST00000260197.11:c.4664T=	ENSP00000260197.6:p.Val1555=
ENST00000525532.5:c.1496T=	ENSP00000434634.1:p.Val499=
ENST00000527934.1:c.509T=	ENSP00000435405.1:p.Val170=
ENST00000532694.5:c.1202T=	ENSP00000432131.1:p.Val401=
ENST00000534286.5:c.1394T=	ENSP00000436447.1:p.Val465=
NM_003105.5:c.4664T=	NP_003096.1:p.Val1555=
XM_011542963.1:c.4550T=	XP_011541265.1:p.Val1517=
XM_011542964.1:c.4664T=	XP_011541266.1:p.Val1555=
XM_011542965.1:c.3125T=	XP_011541267.1:p.Val1042=
XM_011542966.1:c.2024T=	XP_011541268.1:p.Val675=
XM_011542967.1:c.1496T=	XP_011541269.1:p.Val499=
XM_011542963.3:c.4550T=	XP_011541265.1:p.Val1517=
XM_011542965.3:c.3125T=	XP_011541267.1:p.Val1042=
XM_011542967.3:c.1496T=	XP_011541269.1:p.Val499=
XM_017018169.2:c.4352T=	XP_016873658.1:p.Val1451=
XM_017018170.2:c.4139T=	XP_016873659.1:p.Val1380=
XM_017018171.1:c.4664T=	XP_016873660.1:p.Val1555=
XM_017018172.2:c.2024T=	XP_016873661.1:p.Val675=
NM_003105.6:c.4664T= MANE Select	NP_003096.2:p.Val1555=