Canonical Allele Identifier: CA1538218678

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984612G= , CM000667.2:g.33984612G=	GRCh38
NC_000005.9:g.33984717G= , CM000667.1:g.33984717G=	GRCh37
NC_000005.8:g.34020474G=	NCBI36
NG_011691.2:g.5064C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.-29C= MANE Select	ENSP00000296589.4:n.-29C=
ENST00000296589.8:c.-29C=	ENSP00000296589.4:n.-29C=
ENST00000382102.7:c.-29C=	ENSP00000371534.3:n.-29C=
ENST00000509381.1:c.-29C=	ENSP00000421100.1:n.-29C=
NM_001012509.3:c.-29C=	NP_001012527.1:n.-29C=
NM_001297417.2:c.-29C=	NP_001284346.2:n.-29C=
NM_016180.4:c.-29C=	NP_057264.3:n.-29C=
XM_011514052.1:c.-29C=	XP_011512354.1:n.-29C=
XR_925620.1:n.533C=
NM_016180.5:c.-29C= MANE Select	NP_057264.4:n.-29C=
NM_001012509.4:c.-29C=	NP_001012527.2:n.-29C=
NM_001297417.3:c.-29C=	NP_001284346.2:n.-29C=
NM_001297417.4:c.-29C=	NP_001284346.2:n.-29C=