Canonical Allele Identifier: CA387235281
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814908A>T , CM000674.2:g.128814908A>T GRCh38
NC_000012.11:g.129299453A>T , CM000674.1:g.129299453A>T GRCh37
NC_000012.10:g.127865406A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.709T>A MANE Select ENSP00000266771.5:p.Phe237Ile
ENST00000266771.9:c.709T>A ENSP00000266771.5:p.Phe237Ile
ENST00000366292.6:n.1021T>A
ENST00000376740.8:c.288T>A
ENST00000376744.8:c.545T>A
ENST00000539703.1:n.359T>A
ENST00000614634.1:c.-134T>A ENSP00000483143.1:n.-134T>A
NM_145648.3:c.709T>A NP_663623.1:p.Phe237Ile
XM_011537895.1:c.859T>A XP_011536197.1:p.Phe287Ile
XR_429081.2:n.732T>A
XR_944494.1:n.882T>A
XR_944495.1:n.882T>A
XR_944496.1:n.882T>A
XR_944497.1:n.882T>A
XM_017018791.1:c.859T>A XP_016874280.1:p.Phe287Ile
XM_017018792.1:c.859T>A XP_016874281.1:p.Phe287Ile
XM_017018793.1:c.709T>A XP_016874282.1:p.Phe237Ile
XR_002957287.1:n.732T>A
XR_944496.2:n.882T>A
NM_145648.4:c.709T>A MANE Select NP_663623.1:p.Phe237Ile