Canonical Allele Identifier: CA1538218494

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984282_33984283delinsCG , CM000667.2:g.33984282_33984283delinsCG	GRCh38
NC_000005.9:g.33984387_33984388delinsCG , CM000667.1:g.33984387_33984388delinsCG	GRCh37
NC_000005.8:g.34020144_34020145delinsCG	NCBI36
NG_011691.2:g.5393_5394delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.301_302delinsCG MANE Select	ENSP00000296589.4:p.Arg101=
ENST00000296589.8:c.301_302delinsCG	ENSP00000296589.4:p.Arg101=
ENST00000382102.7:c.301_302delinsCG	ENSP00000371534.3:p.Arg101=
ENST00000505056.1:n.280_281delinsCG
ENST00000509381.1:c.301_302delinsCG	ENSP00000421100.1:p.Arg101=
NM_001012509.3:c.301_302delinsCG	NP_001012527.1:p.Arg101=
NM_001297417.2:c.301_302delinsCG	NP_001284346.2:p.Arg101=
NM_016180.4:c.301_302delinsCG	NP_057264.3:p.Arg101=
XM_011514052.1:c.301_302delinsCG	XP_011512354.1:p.Arg101=
XR_925620.1:n.862_863delinsCG
NM_016180.5:c.301_302delinsCG MANE Select	NP_057264.4:p.Arg101=
NM_001012509.4:c.301_302delinsCG	NP_001012527.2:p.Arg101=
NM_001297417.3:c.301_302delinsCG	NP_001284346.2:p.Arg101=
NM_001297417.4:c.301_302delinsCG	NP_001284346.2:p.Arg101=