Canonical Allele Identifier: CA1538218616

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984491G= , CM000667.2:g.33984491G=	GRCh38
NC_000005.9:g.33984596G= , CM000667.1:g.33984596G=	GRCh37
NC_000005.8:g.34020353G=	NCBI36
NG_011691.2:g.5185C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.93C= MANE Select	ENSP00000296589.4:p.Pro31=
ENST00000296589.8:c.93C=	ENSP00000296589.4:p.Pro31=
ENST00000382102.7:c.93C=	ENSP00000371534.3:p.Pro31=
ENST00000505056.1:n.72C=
ENST00000509381.1:c.93C=	ENSP00000421100.1:p.Pro31=
NM_001012509.3:c.93C=	NP_001012527.1:p.Pro31=
NM_001297417.2:c.93C=	NP_001284346.2:p.Pro31=
NM_016180.4:c.93C=	NP_057264.3:p.Pro31=
XM_011514052.1:c.93C=	XP_011512354.1:p.Pro31=
XR_925620.1:n.654C=
NM_016180.5:c.93C= MANE Select	NP_057264.4:p.Pro31=
NM_001012509.4:c.93C=	NP_001012527.2:p.Pro31=
NM_001297417.3:c.93C=	NP_001284346.2:p.Pro31=
NM_001297417.4:c.93C=	NP_001284346.2:p.Pro31=