Canonical Allele Identifier: CA387234748
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814793C>A , CM000674.2:g.128814793C>A GRCh38
NC_000012.11:g.129299338C>A , CM000674.1:g.129299338C>A GRCh37
NC_000012.10:g.127865291C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.824G>T MANE Select ENSP00000266771.5:p.Gly275Val
ENST00000266771.9:c.824G>T ENSP00000266771.5:p.Gly275Val
ENST00000366292.6:n.1136G>T
ENST00000376740.8:c.403G>T
ENST00000376744.8:c.660G>T
ENST00000539703.1:n.474G>T
ENST00000614634.1:c.-19G>T ENSP00000483143.1:n.-19G>T
NM_145648.3:c.824G>T NP_663623.1:p.Gly275Val
XM_011537895.1:c.974G>T XP_011536197.1:p.Gly325Val
XR_429081.2:n.847G>T
XR_944494.1:n.997G>T
XR_944495.1:n.997G>T
XR_944496.1:n.997G>T
XR_944497.1:n.997G>T
XM_017018791.1:c.974G>T XP_016874280.1:p.Gly325Val
XM_017018792.1:c.974G>T XP_016874281.1:p.Gly325Val
XM_017018793.1:c.824G>T XP_016874282.1:p.Gly275Val
XR_002957287.1:n.847G>T
XR_944496.2:n.997G>T
NM_145648.4:c.824G>T MANE Select NP_663623.1:p.Gly275Val