Canonical Allele Identifier: CA477218143

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121393647T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121522938T>C , CM000673.2:g.121522938T>C	GRCh38
NC_000011.9:g.121393647T>C , CM000673.1:g.121393647T>C	GRCh37
NC_000011.8:g.120898857T>C	NCBI36
NG_023313.1:g.75687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260197.12:c.1545T>C MANE Select	ENSP00000260197.6:p.Ala515=
ENST00000260197.11:c.1545T>C	ENSP00000260197.6:p.Ala515=
ENST00000532451.1:n.1497T>C
NM_003105.5:c.1545T>C	NP_003096.1:p.Ala515=
XM_011542963.1:c.1545T>C	XP_011541265.1:p.Ala515=
XM_011542964.1:c.1545T>C	XP_011541266.1:p.Ala515=
XM_011542965.1:c.-78T>C	XP_011541267.1:n.-78T>C
XM_011542963.3:c.1545T>C	XP_011541265.1:p.Ala515=
XM_011542965.3:c.-78T>C	XP_011541267.1:n.-78T>C
XM_017018169.2:c.1233T>C	XP_016873658.1:p.Ala411=
XM_017018170.2:c.1020T>C	XP_016873659.1:p.Ala340=
XM_017018171.1:c.1545T>C	XP_016873660.1:p.Ala515=
NM_003105.6:c.1545T>C MANE Select	NP_003096.2:p.Ala515=