Canonical Allele Identifier: CA2071402358

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815067T= , CM000674.2:g.128815067T=	GRCh38
NC_000012.11:g.129299612T= , CM000674.1:g.129299612T=	GRCh37
NC_000012.10:g.127865565T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.550A= MANE Select	ENSP00000266771.5:p.Lys184=
ENST00000266771.9:c.550A=	ENSP00000266771.5:p.Lys184=
ENST00000366292.6:n.862A=
ENST00000376740.8:c.129A=
ENST00000376744.8:c.386A=
ENST00000535272.1:n.344A=
ENST00000539703.1:n.200A=
NM_145648.3:c.550A=	NP_663623.1:p.Lys184=
XM_011537895.1:c.700A=	XP_011536197.1:p.Lys234=
XR_429081.2:n.573A=
XR_944494.1:n.723A=
XR_944495.1:n.723A=
XR_944496.1:n.723A=
XR_944497.1:n.723A=
XM_017018791.1:c.700A=	XP_016874280.1:p.Lys234=
XM_017018792.1:c.700A=	XP_016874281.1:p.Lys234=
XM_017018793.1:c.550A=	XP_016874282.1:p.Lys184=
XR_002957287.1:n.573A=
XR_944496.2:n.723A=
NM_145648.4:c.550A= MANE Select	NP_663623.1:p.Lys184=