Canonical Allele Identifier: CA2765834771

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964099_33964113del , CM000667.2:g.33964099_33964113del	GRCh38
NC_000005.9:g.33964204_33964218del , CM000667.1:g.33964204_33964218del	GRCh37
NC_000005.8:g.33999961_33999975del	NCBI36
NG_011691.2:g.25564_25578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-96_563-82del MANE Select	ENSP00000296589.4:n.563-96_563-82del
ENST00000296589.8:c.563-96_563-82del	ENSP00000296589.4:n.563-96_563-82del
ENST00000382102.7:c.563-96_563-82del	ENSP00000371534.3:n.563-96_563-82del
ENST00000505056.1:n.365-96_365-82del
ENST00000509381.1:c.563-9608_563-9594del	ENSP00000421100.1:n.563-9608_563-9594del
ENST00000510600.1:c.38-96_38-82del	ENSP00000424010.1:n.38-96_38-82del
NM_001012509.3:c.563-96_563-82del	NP_001012527.1:n.563-96_563-82del
NM_001297417.2:c.563-9608_563-9594del	NP_001284346.2:n.563-9608_563-9594del
NM_016180.4:c.563-96_563-82del	NP_057264.3:n.563-96_563-82del
XM_011514051.1:c.161-96_161-82del	XP_011512353.1:n.161-96_161-82del
XM_011514052.1:c.563-96_563-82del	XP_011512354.1:n.563-96_563-82del
XR_925620.1:n.1380-96_1380-82del
NM_016180.5:c.563-96_563-82del MANE Select	NP_057264.4:n.563-96_563-82del
NM_001012509.4:c.563-96_563-82del	NP_001012527.2:n.563-96_563-82del
NM_001297417.3:c.563-9608_563-9594del	NP_001284346.2:n.563-9608_563-9594del
NM_001297417.4:c.563-9608_563-9594del	NP_001284346.2:n.563-9608_563-9594del