Canonical Allele Identifier: CA2614035598

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62999214-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62999217dup , CM000673.2:g.62999217dup	GRCh38
NC_000011.9:g.62766689dup , CM000673.1:g.62766689dup	GRCh37
NC_000011.8:g.62523265dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.593-126dup MANE Select	ENSP00000337335.2:n.593-126dup
ENST00000311438.12:c.593-126dup	ENSP00000311463.8:n.593-126dup
ENST00000336232.6:c.593-126dup	ENSP00000337335.2:n.593-126dup
ENST00000430500.6:c.593-126dup	ENSP00000398548.2:n.593-126dup
ENST00000535878.5:c.224-126dup	ENSP00000443368.1:n.224-126dup
ENST00000539841.1:n.285dup
ENST00000542795.5:n.314-126dup
ENST00000542904.1:n.433-126dup
ENST00000545207.5:c.320-126dup	ENSP00000441658.1:n.320-126dup
NM_001184732.1:c.593-126dup	NP_001171661.1:n.593-126dup
NM_001184733.1:c.320-126dup	NP_001171662.1:n.320-126dup
NM_001184736.1:c.224-126dup	NP_001171665.1:n.224-126dup
NM_004254.3:c.593-126dup	NP_004245.2:n.593-126dup
XM_011545364.1:c.224-126dup	XP_011543666.1:n.224-126dup
NM_004254.4:c.593-126dup MANE Select	NP_004245.2:n.593-126dup
NM_001184732.2:c.593-126dup	NP_001171661.1:n.593-126dup
NM_001184733.2:c.320-126dup	NP_001171662.1:n.320-126dup
NM_001184736.2:c.224-126dup	NP_001171665.1:n.224-126dup