Canonical Allele Identifier: CA2071401717

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814779T= , CM000674.2:g.128814779T=	GRCh38
NC_000012.11:g.129299324T= , CM000674.1:g.129299324T=	GRCh37
NC_000012.10:g.127865277T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.838A= MANE Select	ENSP00000266771.5:p.Asn280=
ENST00000266771.9:c.838A=	ENSP00000266771.5:p.Asn280=
ENST00000366292.6:n.1150A=
ENST00000376740.8:c.417A=
ENST00000376744.8:c.674A=
ENST00000539703.1:n.488A=
ENST00000614634.1:c.-5A=	ENSP00000483143.1:n.-5A=
NM_145648.3:c.838A=	NP_663623.1:p.Asn280=
XM_011537895.1:c.988A=	XP_011536197.1:p.Asn330=
XR_429081.2:n.861A=
XR_944494.1:n.1011A=
XR_944495.1:n.1011A=
XR_944496.1:n.1011A=
XR_944497.1:n.1011A=
XM_017018791.1:c.988A=	XP_016874280.1:p.Asn330=
XM_017018792.1:c.988A=	XP_016874281.1:p.Asn330=
XM_017018793.1:c.838A=	XP_016874282.1:p.Asn280=
XR_002957287.1:n.861A=
XR_944496.2:n.1011A=
NM_145648.4:c.838A= MANE Select	NP_663623.1:p.Asn280=