Canonical Allele Identifier: CA2071402269

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815026C= , CM000674.2:g.128815026C=	GRCh38
NC_000012.11:g.129299571C= , CM000674.1:g.129299571C=	GRCh37
NC_000012.10:g.127865524C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.591G= MANE Select	ENSP00000266771.5:p.Trp197=
ENST00000266771.9:c.591G=	ENSP00000266771.5:p.Trp197=
ENST00000366292.6:n.903G=
ENST00000376740.8:c.170G=
ENST00000376744.8:c.427G=
ENST00000535272.1:n.385G=
ENST00000539703.1:n.241G=
NM_145648.3:c.591G=	NP_663623.1:p.Trp197=
XM_011537895.1:c.741G=	XP_011536197.1:p.Trp247=
XR_429081.2:n.614G=
XR_944494.1:n.764G=
XR_944495.1:n.764G=
XR_944496.1:n.764G=
XR_944497.1:n.764G=
XM_017018791.1:c.741G=	XP_016874280.1:p.Trp247=
XM_017018792.1:c.741G=	XP_016874281.1:p.Trp247=
XM_017018793.1:c.591G=	XP_016874282.1:p.Trp197=
XR_002957287.1:n.614G=
XR_944496.2:n.764G=
NM_145648.4:c.591G= MANE Select	NP_663623.1:p.Trp197=