Canonical Allele Identifier: CA1538196378

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964010C= , CM000667.2:g.33964010C=	GRCh38
NC_000005.9:g.33964115C= , CM000667.1:g.33964115C=	GRCh37
NC_000005.8:g.33999872C=	NCBI36
NG_011691.2:g.25666G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.569G= MANE Select	ENSP00000296589.4:p.Gly190=
ENST00000296589.8:c.569G=	ENSP00000296589.4:p.Gly190=
ENST00000382102.7:c.569G=	ENSP00000371534.3:p.Gly190=
ENST00000505056.1:n.371G=
ENST00000509381.1:c.563-9506G=	ENSP00000421100.1:n.563-9506G=
ENST00000510600.1:c.44G=	ENSP00000424010.1:p.Gly15=
NM_001012509.3:c.569G=	NP_001012527.1:p.Gly190=
NM_001297417.2:c.563-9506G=	NP_001284346.2:n.563-9506G=
NM_016180.4:c.569G=	NP_057264.3:p.Gly190=
XM_011514051.1:c.167G=	XP_011512353.1:p.Gly56=
XM_011514052.1:c.569G=	XP_011512354.1:p.Gly190=
XR_925620.1:n.1386G=
NM_016180.5:c.569G= MANE Select	NP_057264.4:p.Gly190=
NM_001012509.4:c.569G=	NP_001012527.2:p.Gly190=
NM_001297417.3:c.563-9506G=	NP_001284346.2:n.563-9506G=
NM_001297417.4:c.563-9506G=	NP_001284346.2:n.563-9506G=