Canonical Allele Identifier: CA1538196369

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964008_33964009delinsCT , CM000667.2:g.33964008_33964009delinsCT	GRCh38
NC_000005.9:g.33964113_33964114delinsCT , CM000667.1:g.33964113_33964114delinsCT	GRCh37
NC_000005.8:g.33999870_33999871delinsCT	NCBI36
NG_011691.2:g.25667_25668delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.570_571delinsAG MANE Select	ENSP00000296589.4:p.Gly190=
ENST00000296589.8:c.570_571delinsAG	ENSP00000296589.4:p.Gly190=
ENST00000382102.7:c.570_571delinsAG	ENSP00000371534.3:p.Gly190=
ENST00000505056.1:n.372_373delinsAG
ENST00000509381.1:c.563-9505_563-9504delinsAG	ENSP00000421100.1:n.563-9505_563-9504delinsAG
ENST00000510600.1:c.45_46delinsAG	ENSP00000424010.1:p.Gly15=
NM_001012509.3:c.570_571delinsAG	NP_001012527.1:p.Gly190=
NM_001297417.2:c.563-9505_563-9504delinsAG	NP_001284346.2:n.563-9505_563-9504delinsAG
NM_016180.4:c.570_571delinsAG	NP_057264.3:p.Gly190=
XM_011514051.1:c.168_169delinsAG	XP_011512353.1:p.Gly56=
XM_011514052.1:c.570_571delinsAG	XP_011512354.1:p.Gly190=
XR_925620.1:n.1387_1388delinsAG
NM_016180.5:c.570_571delinsAG MANE Select	NP_057264.4:p.Gly190=
NM_001012509.4:c.570_571delinsAG	NP_001012527.2:p.Gly190=
NM_001297417.3:c.563-9505_563-9504delinsAG	NP_001284346.2:n.563-9505_563-9504delinsAG
NM_001297417.4:c.563-9505_563-9504delinsAG	NP_001284346.2:n.563-9505_563-9504delinsAG