Canonical Allele Identifier: CA1538211694

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951592C= , CM000667.2:g.33951592C=	GRCh38
NC_000005.9:g.33951697C= , CM000667.1:g.33951697C=	GRCh37
NC_000005.8:g.33987454C=	NCBI36
NG_011691.2:g.38084G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296589.9:c.1118G= MANE Select	ENSP00000296589.4:p.Gly373=
ENST00000296589.8:c.1118G=	ENSP00000296589.4:p.Gly373=
ENST00000382102.7:c.1118G=	ENSP00000371534.3:p.Gly373=
ENST00000509381.1:c.*60G=	ENSP00000421100.1:n.*60G=
ENST00000510600.1:c.593G=	ENSP00000424010.1:p.Gly198=
NM_001012509.3:c.1118G=	NP_001012527.1:p.Gly373=
NM_001297417.2:c.*60G=	NP_001284346.2:n.*60G=
NM_016180.4:c.1118G=	NP_057264.3:p.Gly373=
XM_011514051.1:c.716G=	XP_011512353.1:p.Gly239=
XR_925620.1:n.1935G=
NM_016180.5:c.1118G= MANE Select	NP_057264.4:p.Gly373=
NM_001012509.4:c.1118G=	NP_001012527.2:p.Gly373=
NM_001297417.3:c.*60G=	NP_001284346.2:n.*60G=
NM_001297417.4:c.*60G=	NP_001284346.2:n.*60G=