Canonical Allele Identifier: CA1538195661

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963649A= , CM000667.2:g.33963649A=	GRCh38
NC_000005.9:g.33963754A= , CM000667.1:g.33963754A=	GRCh37
NC_000005.8:g.33999511A=	NCBI36
NG_011691.2:g.26027T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.888+42T= MANE Select	ENSP00000296589.4:n.888+42T=
ENST00000296589.8:c.888+42T=	ENSP00000296589.4:n.888+42T=
ENST00000382102.7:c.888+42T=	ENSP00000371534.3:n.888+42T=
ENST00000505056.1:n.732T=
ENST00000509381.1:c.563-9145T=	ENSP00000421100.1:n.563-9145T=
ENST00000510600.1:c.363+42T=	ENSP00000424010.1:n.363+42T=
NM_001012509.3:c.888+42T=	NP_001012527.1:n.888+42T=
NM_001297417.2:c.563-9145T=	NP_001284346.2:n.563-9145T=
NM_016180.4:c.888+42T=	NP_057264.3:n.888+42T=
XM_011514051.1:c.486+42T=	XP_011512353.1:n.486+42T=
XM_011514052.1:c.888+42T=	XP_011512354.1:n.888+42T=
XR_925620.1:n.1705+42T=
NM_016180.5:c.888+42T= MANE Select	NP_057264.4:n.888+42T=
NM_001012509.4:c.888+42T=	NP_001012527.2:n.888+42T=
NM_001297417.3:c.563-9145T=	NP_001284346.2:n.563-9145T=
NM_001297417.4:c.563-9145T=	NP_001284346.2:n.563-9145T=