Canonical Allele Identifier: CA2004916762

Gene: SORL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121552707G= , CM000673.2:g.121552707G=	GRCh38
NC_000011.9:g.121423416G= , CM000673.1:g.121423416G=	GRCh37
NC_000011.8:g.120928626G=	NCBI36
NG_023313.1:g.105456G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.2267-1230G= MANE Select	ENSP00000260197.6:n.2267-1230G=
ENST00000260197.11:c.2267-1230G=	ENSP00000260197.6:n.2267-1230G=
NM_003105.5:c.2267-1230G=	NP_003096.1:n.2267-1230G=
XM_011542963.1:c.2267-1230G=	XP_011541265.1:n.2267-1230G=
XM_011542964.1:c.2267-1230G=	XP_011541266.1:n.2267-1230G=
XM_011542965.1:c.728-1230G=	XP_011541267.1:n.728-1230G=
XM_011542963.3:c.2267-1230G=	XP_011541265.1:n.2267-1230G=
XM_011542965.3:c.728-1230G=	XP_011541267.1:n.728-1230G=
XM_017018169.2:c.1955-1230G=	XP_016873658.1:n.1955-1230G=
XM_017018170.2:c.1742-1230G=	XP_016873659.1:n.1742-1230G=
XM_017018171.1:c.2267-1230G=	XP_016873660.1:n.2267-1230G=
XM_017018172.2:c.-282-1230G=	XP_016873661.1:n.-282-1230G=
NM_003105.6:c.2267-1230G= MANE Select	NP_003096.2:n.2267-1230G=