Canonical Allele Identifier: CA1538218516

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984319_33984320delinsCG , CM000667.2:g.33984319_33984320delinsCG	GRCh38
NC_000005.9:g.33984424_33984425delinsCG , CM000667.1:g.33984424_33984425delinsCG	GRCh37
NC_000005.8:g.34020181_34020182delinsCG	NCBI36
NG_011691.2:g.5356_5357delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.264_265delinsCG MANE Select	ENSP00000296589.4:p.Val88=
ENST00000296589.8:c.264_265delinsCG	ENSP00000296589.4:p.Val88=
ENST00000382102.7:c.264_265delinsCG	ENSP00000371534.3:p.Val88=
ENST00000505056.1:n.243_244delinsCG
ENST00000509381.1:c.264_265delinsCG	ENSP00000421100.1:p.Val88=
NM_001012509.3:c.264_265delinsCG	NP_001012527.1:p.Val88=
NM_001297417.2:c.264_265delinsCG	NP_001284346.2:p.Val88=
NM_016180.4:c.264_265delinsCG	NP_057264.3:p.Val88=
XM_011514052.1:c.264_265delinsCG	XP_011512354.1:p.Val88=
XR_925620.1:n.825_826delinsCG
NM_016180.5:c.264_265delinsCG MANE Select	NP_057264.4:p.Val88=
NM_001012509.4:c.264_265delinsCG	NP_001012527.2:p.Val88=
NM_001297417.3:c.264_265delinsCG	NP_001284346.2:p.Val88=
NM_001297417.4:c.264_265delinsCG	NP_001284346.2:p.Val88=