Canonical Allele Identifier: CA2071402295

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815037A= , CM000674.2:g.128815037A=	GRCh38
NC_000012.11:g.129299582A= , CM000674.1:g.129299582A=	GRCh37
NC_000012.10:g.127865535A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.580T= MANE Select	ENSP00000266771.5:p.Phe194=
ENST00000266771.9:c.580T=	ENSP00000266771.5:p.Phe194=
ENST00000366292.6:n.892T=
ENST00000376740.8:c.159T=
ENST00000376744.8:c.416T=
ENST00000535272.1:n.374T=
ENST00000539703.1:n.230T=
NM_145648.3:c.580T=	NP_663623.1:p.Phe194=
XM_011537895.1:c.730T=	XP_011536197.1:p.Phe244=
XR_429081.2:n.603T=
XR_944494.1:n.753T=
XR_944495.1:n.753T=
XR_944496.1:n.753T=
XR_944497.1:n.753T=
XM_017018791.1:c.730T=	XP_016874280.1:p.Phe244=
XM_017018792.1:c.730T=	XP_016874281.1:p.Phe244=
XM_017018793.1:c.580T=	XP_016874282.1:p.Phe194=
XR_002957287.1:n.603T=
XR_944496.2:n.753T=
NM_145648.4:c.580T= MANE Select	NP_663623.1:p.Phe194=