Canonical Allele Identifier: CA2071401824

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814801C= , CM000674.2:g.128814801C=	GRCh38
NC_000012.11:g.129299346C= , CM000674.1:g.129299346C=	GRCh37
NC_000012.10:g.127865299C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.816G= MANE Select	ENSP00000266771.5:p.Lys272=
ENST00000266771.9:c.816G=	ENSP00000266771.5:p.Lys272=
ENST00000366292.6:n.1128G=
ENST00000376740.8:c.395G=
ENST00000376744.8:c.652G=
ENST00000539703.1:n.466G=
ENST00000614634.1:c.-27G=	ENSP00000483143.1:n.-27G=
NM_145648.3:c.816G=	NP_663623.1:p.Lys272=
XM_011537895.1:c.966G=	XP_011536197.1:p.Lys322=
XR_429081.2:n.839G=
XR_944494.1:n.989G=
XR_944495.1:n.989G=
XR_944496.1:n.989G=
XR_944497.1:n.989G=
XM_017018791.1:c.966G=	XP_016874280.1:p.Lys322=
XM_017018792.1:c.966G=	XP_016874281.1:p.Lys322=
XM_017018793.1:c.816G=	XP_016874282.1:p.Lys272=
XR_002957287.1:n.839G=
XR_944496.2:n.989G=
NM_145648.4:c.816G= MANE Select	NP_663623.1:p.Lys272=