Canonical Allele Identifier: CA2071401680
Gene: SLC15A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814755G= , CM000674.2:g.128814755G= GRCh38
NC_000012.11:g.129299300G= , CM000674.1:g.129299300G= GRCh37
NC_000012.10:g.127865253G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266771.10:c.842+20C= MANE Select ENSP00000266771.5:n.842+20C=
ENST00000266771.9:c.842+20C= ENSP00000266771.5:n.842+20C=
ENST00000366292.6:n.1154+20C=
ENST00000376740.8:c.421+20C=
ENST00000376744.8:c.678+20C=
ENST00000539703.1:n.492+20C=
ENST00000614634.1:c.-1+20C= ENSP00000483143.1:n.-1+20C=
NM_145648.3:c.842+20C= NP_663623.1:n.842+20C=
XM_011537895.1:c.992+20C= XP_011536197.1:n.992+20C=
XR_429081.2:n.865+20C=
XR_944494.1:n.1015+20C=
XR_944495.1:n.1015+20C=
XR_944496.1:n.1015+20C=
XR_944497.1:n.1015+20C=
XM_017018791.1:c.992+20C= XP_016874280.1:n.992+20C=
XM_017018792.1:c.992+20C= XP_016874281.1:n.992+20C=
XM_017018793.1:c.842+20C= XP_016874282.1:n.842+20C=
XR_002957287.1:n.865+20C=
XR_944496.2:n.1015+20C=
NM_145648.4:c.842+20C= MANE Select NP_663623.1:n.842+20C=