Canonical Allele Identifier: CA1397722668

Gene: SLC15A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121929321G= , CM000665.2:g.121929321G=	GRCh38
NC_000003.11:g.121648168G= , CM000665.1:g.121648168G=	GRCh37
NC_000003.10:g.123130858G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021082.4:c.1526G= MANE Select	NP_066568.3:p.Arg509=
ENST00000489711.6:c.1526G= MANE Select	ENSP00000417085.1:p.Arg509=
NM_001145998.1:c.1433G=	NP_001139470.1:p.Arg478=
NM_001145998.2:c.1433G=	NP_001139470.1:p.Arg478=
NM_021082.3:c.1526G=	NP_066568.3:p.Arg509=
ENST00000295605.6:c.1433G=	ENSP00000295605.2:p.Arg478=
ENST00000465060.1:n.449G=
ENST00000489711.5:c.1526G=	ENSP00000417085.1:p.Arg509=
XM_005247722.2:c.1526G=	XP_005247779.1:p.Arg509=
XM_005247722.3:c.1526G=	XP_005247779.1:p.Arg509=
XM_006713736.2:c.1526G=	XP_006713799.1:p.Arg509=
XM_006713736.3:c.1526G=	XP_006713799.1:p.Arg509=