Canonical Allele Identifier: CA2071401946

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814856C= , CM000674.2:g.128814856C=	GRCh38
NC_000012.11:g.129299401C= , CM000674.1:g.129299401C=	GRCh37
NC_000012.10:g.127865354C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.761G= MANE Select	ENSP00000266771.5:p.Gly254=
ENST00000266771.9:c.761G=	ENSP00000266771.5:p.Gly254=
ENST00000366292.6:n.1073G=
ENST00000376740.8:c.340G=
ENST00000376744.8:c.597G=
ENST00000539703.1:n.411G=
ENST00000614634.1:c.-82G=	ENSP00000483143.1:n.-82G=
NM_145648.3:c.761G=	NP_663623.1:p.Gly254=
XM_011537895.1:c.911G=	XP_011536197.1:p.Gly304=
XR_429081.2:n.784G=
XR_944494.1:n.934G=
XR_944495.1:n.934G=
XR_944496.1:n.934G=
XR_944497.1:n.934G=
XM_017018791.1:c.911G=	XP_016874280.1:p.Gly304=
XM_017018792.1:c.911G=	XP_016874281.1:p.Gly304=
XM_017018793.1:c.761G=	XP_016874282.1:p.Gly254=
XR_002957287.1:n.784G=
XR_944496.2:n.934G=
NM_145648.4:c.761G= MANE Select	NP_663623.1:p.Gly254=