Canonical Allele Identifier: CA387235328
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814935T>A , CM000674.2:g.128814935T>A GRCh38
NC_000012.11:g.129299480T>A , CM000674.1:g.129299480T>A GRCh37
NC_000012.10:g.127865433T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.682A>T MANE Select ENSP00000266771.5:p.Ile228Phe
ENST00000266771.9:c.682A>T ENSP00000266771.5:p.Ile228Phe
ENST00000366292.6:n.994A>T
ENST00000376740.8:c.261A>T
ENST00000376744.8:c.518A>T
ENST00000539703.1:n.332A>T
ENST00000614634.1:c.-161A>T ENSP00000483143.1:n.-161A>T
NM_145648.3:c.682A>T NP_663623.1:p.Ile228Phe
XM_011537895.1:c.832A>T XP_011536197.1:p.Ile278Phe
XR_429081.2:n.705A>T
XR_944494.1:n.855A>T
XR_944495.1:n.855A>T
XR_944496.1:n.855A>T
XR_944497.1:n.855A>T
XM_017018791.1:c.832A>T XP_016874280.1:p.Ile278Phe
XM_017018792.1:c.832A>T XP_016874281.1:p.Ile278Phe
XM_017018793.1:c.682A>T XP_016874282.1:p.Ile228Phe
XR_002957287.1:n.705A>T
XR_944496.2:n.855A>T
NM_145648.4:c.682A>T MANE Select NP_663623.1:p.Ile228Phe