Canonical Allele Identifier: CA387235439
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814986C>A , CM000674.2:g.128814986C>A GRCh38
NC_000012.11:g.129299531C>A , CM000674.1:g.129299531C>A GRCh37
NC_000012.10:g.127865484C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.631G>T MANE Select ENSP00000266771.5:p.Gly211Cys
ENST00000266771.9:c.631G>T ENSP00000266771.5:p.Gly211Cys
ENST00000366292.6:n.943G>T
ENST00000376740.8:c.210G>T
ENST00000376744.8:c.467G>T
ENST00000535272.1:n.425G>T
ENST00000539703.1:n.281G>T
NM_145648.3:c.631G>T NP_663623.1:p.Gly211Cys
XM_011537895.1:c.781G>T XP_011536197.1:p.Gly261Cys
XR_429081.2:n.654G>T
XR_944494.1:n.804G>T
XR_944495.1:n.804G>T
XR_944496.1:n.804G>T
XR_944497.1:n.804G>T
XM_017018791.1:c.781G>T XP_016874280.1:p.Gly261Cys
XM_017018792.1:c.781G>T XP_016874281.1:p.Gly261Cys
XM_017018793.1:c.631G>T XP_016874282.1:p.Gly211Cys
XR_002957287.1:n.654G>T
XR_944496.2:n.804G>T
NM_145648.4:c.631G>T MANE Select NP_663623.1:p.Gly211Cys