Canonical Allele Identifier: CA474857062

Gene: SLC22A8

Linked Data

• MyVariant Identifiers: chr11:g.62766442G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998970G>A , CM000673.2:g.62998970G>A	GRCh38
NC_000011.9:g.62766442G>A , CM000673.1:g.62766442G>A	GRCh37
NC_000011.8:g.62523018G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.712C>T MANE Select	ENSP00000337335.2:p.Leu238=
ENST00000311438.12:c.712C>T	ENSP00000311463.8:p.Leu238=
ENST00000336232.6:c.712C>T	ENSP00000337335.2:p.Leu238=
ENST00000430500.6:c.712C>T	ENSP00000398548.2:p.Leu238=
ENST00000535878.5:c.343C>T	ENSP00000443368.1:p.Leu115=
ENST00000539841.1:n.530C>T
ENST00000542795.5:n.433C>T
ENST00000542904.1:n.552C>T
ENST00000545207.5:c.439C>T	ENSP00000441658.1:p.Leu147=
NM_001184732.1:c.712C>T	NP_001171661.1:p.Leu238=
NM_001184733.1:c.439C>T	NP_001171662.1:p.Leu147=
NM_001184736.1:c.343C>T	NP_001171665.1:p.Leu115=
NM_004254.3:c.712C>T	NP_004245.2:p.Leu238=
XM_011545364.1:c.343C>T	XP_011543666.1:p.Leu115=
NM_004254.4:c.712C>T MANE Select	NP_004245.2:p.Leu238=
NM_001184732.2:c.712C>T	NP_001171661.1:p.Leu238=
NM_001184733.2:c.439C>T	NP_001171662.1:p.Leu147=
NM_001184736.2:c.343C>T	NP_001171665.1:p.Leu115=