Canonical Allele Identifier: CA2071401714
Gene: SLC15A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814777A= , CM000674.2:g.128814777A= GRCh38
NC_000012.11:g.129299322A= , CM000674.1:g.129299322A= GRCh37
NC_000012.10:g.127865275A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266771.10:c.840T= MANE Select ENSP00000266771.5:p.Asn280=
ENST00000266771.9:c.840T= ENSP00000266771.5:p.Asn280=
ENST00000366292.6:n.1152T=
ENST00000376740.8:c.419T=
ENST00000376744.8:c.676T=
ENST00000539703.1:n.490T=
ENST00000614634.1:c.-3T= ENSP00000483143.1:n.-3T=
NM_145648.3:c.840T= NP_663623.1:p.Asn280=
XM_011537895.1:c.990T= XP_011536197.1:p.Asn330=
XR_429081.2:n.863T=
XR_944494.1:n.1013T=
XR_944495.1:n.1013T=
XR_944496.1:n.1013T=
XR_944497.1:n.1013T=
XM_017018791.1:c.990T= XP_016874280.1:p.Asn330=
XM_017018792.1:c.990T= XP_016874281.1:p.Asn330=
XM_017018793.1:c.840T= XP_016874282.1:p.Asn280=
XR_002957287.1:n.863T=
XR_944496.2:n.1013T=
NM_145648.4:c.840T= MANE Select NP_663623.1:p.Asn280=