Canonical Allele Identifier: CA1978013210
Gene: SLC22A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62996071G= , CM000673.2:g.62996071G= GRCh38
NC_000011.9:g.62763543G= , CM000673.1:g.62763543G= GRCh37
NC_000011.8:g.62520119G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336232.7:c.843C= MANE Select ENSP00000337335.2:p.Val281=
ENST00000311438.12:c.843C= ENSP00000311463.8:p.Val281=
ENST00000336232.6:c.843C= ENSP00000337335.2:p.Val281=
ENST00000430500.6:c.843C= ENSP00000398548.2:p.Val281=
ENST00000535878.5:c.474C= ENSP00000443368.1:p.Val158=
ENST00000539841.1:n.661C=
ENST00000545207.5:c.570C= ENSP00000441658.1:p.Val190=
NM_001184732.1:c.843C= NP_001171661.1:p.Val281=
NM_001184733.1:c.570C= NP_001171662.1:p.Val190=
NM_001184736.1:c.474C= NP_001171665.1:p.Val158=
NM_004254.3:c.843C= NP_004245.2:p.Val281=
XM_011545364.1:c.474C= XP_011543666.1:p.Val158=
NM_004254.4:c.843C= MANE Select NP_004245.2:p.Val281=
NM_001184732.2:c.843C= NP_001171661.1:p.Val281=
NM_001184733.2:c.570C= NP_001171662.1:p.Val190=
NM_001184736.2:c.474C= NP_001171665.1:p.Val158=