Canonical Allele Identifier: CA1538196356

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964005C= , CM000667.2:g.33964005C=	GRCh38
NC_000005.9:g.33964110C= , CM000667.1:g.33964110C=	GRCh37
NC_000005.8:g.33999867C=	NCBI36
NG_011691.2:g.25671G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296589.9:c.574G= MANE Select	ENSP00000296589.4:p.Ala192=
ENST00000296589.8:c.574G=	ENSP00000296589.4:p.Ala192=
ENST00000382102.7:c.574G=	ENSP00000371534.3:p.Ala192=
ENST00000505056.1:n.376G=
ENST00000509381.1:c.563-9501G=	ENSP00000421100.1:n.563-9501G=
ENST00000510600.1:c.49G=	ENSP00000424010.1:p.Ala17=
NM_001012509.3:c.574G=	NP_001012527.1:p.Ala192=
NM_001297417.2:c.563-9501G=	NP_001284346.2:n.563-9501G=
NM_016180.4:c.574G=	NP_057264.3:p.Ala192=
XM_011514051.1:c.172G=	XP_011512353.1:p.Ala58=
XM_011514052.1:c.574G=	XP_011512354.1:p.Ala192=
XR_925620.1:n.1391G=
NM_016180.5:c.574G= MANE Select	NP_057264.4:p.Ala192=
NM_001012509.4:c.574G=	NP_001012527.2:p.Ala192=
NM_001297417.3:c.563-9501G=	NP_001284346.2:n.563-9501G=
NM_001297417.4:c.563-9501G=	NP_001284346.2:n.563-9501G=