Canonical Allele Identifier: CA229888632

Gene: SORL1

Linked Data

• dbSNP Id: rs1031898507
• gnomAD v2: 11-121489350-G-C
• gnomAD v3: 11-121618641-G-C
• gnomAD v4: 11-121618641-G-C
• MyVariant Identifiers: chr11:g.121489350G>C (hg19) ; chr11:g.121618641G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121618641G>C , CM000673.2:g.121618641G>C	GRCh38
NC_000011.9:g.121489350G>C , CM000673.1:g.121489350G>C	GRCh37
NC_000011.8:g.120994560G>C	NCBI36
NG_023313.1:g.171390G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.5605-133G>C MANE Select	ENSP00000260197.6:n.5605-133G>C
ENST00000260197.11:c.5605-133G>C	ENSP00000260197.6:n.5605-133G>C
ENST00000524633.1:n.771-133G>C
ENST00000525532.5:c.2437-133G>C	ENSP00000434634.1:n.2437-133G>C
ENST00000527934.1:c.1450-133G>C	ENSP00000435405.1:n.1450-133G>C
ENST00000528339.5:n.3242-133G>C
ENST00000532694.5:c.2143-133G>C	ENSP00000432131.1:n.2143-133G>C
ENST00000534286.5:c.2335-133G>C	ENSP00000436447.1:n.2335-133G>C
ENST00000534754.5:n.1767-133G>C
NM_003105.5:c.5605-133G>C	NP_003096.1:n.5605-133G>C
XM_011542963.1:c.5491-133G>C	XP_011541265.1:n.5491-133G>C
XM_011542965.1:c.4066-133G>C	XP_011541267.1:n.4066-133G>C
XM_011542966.1:c.2965-133G>C	XP_011541268.1:n.2965-133G>C
XM_011542967.1:c.2437-133G>C	XP_011541269.1:n.2437-133G>C
XM_011542963.3:c.5491-133G>C	XP_011541265.1:n.5491-133G>C
XM_011542965.3:c.4066-133G>C	XP_011541267.1:n.4066-133G>C
XM_011542967.3:c.2437-133G>C	XP_011541269.1:n.2437-133G>C
XM_017018169.2:c.5293-133G>C	XP_016873658.1:n.5293-133G>C
XM_017018170.2:c.5080-133G>C	XP_016873659.1:n.5080-133G>C
XM_017018172.2:c.2965-133G>C	XP_016873661.1:n.2965-133G>C
NM_003105.6:c.5605-133G>C MANE Select	NP_003096.2:n.5605-133G>C