Canonical Allele Identifier: CA558967717

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1404760870
• gnomAD v2: 5-33964157-CA-C
• gnomAD v4: 5-33964052-CA-C
• MyVariant Identifiers: chr5:g.33964158del (hg19) ; chr5:g.33964053del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964055del , CM000667.2:g.33964055del	GRCh38
NC_000005.9:g.33964160del , CM000667.1:g.33964160del	GRCh37
NC_000005.8:g.33999917del	NCBI36
NG_011691.2:g.25623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-37del MANE Select	ENSP00000296589.4:n.563-37del
ENST00000296589.8:c.563-37del	ENSP00000296589.4:n.563-37del
ENST00000382102.7:c.563-37del	ENSP00000371534.3:n.563-37del
ENST00000505056.1:n.365-37del
ENST00000509381.1:c.563-9549del	ENSP00000421100.1:n.563-9549del
ENST00000510600.1:c.38-37del	ENSP00000424010.1:n.38-37del
NM_001012509.3:c.563-37del	NP_001012527.1:n.563-37del
NM_001297417.2:c.563-9549del	NP_001284346.2:n.563-9549del
NM_016180.4:c.563-37del	NP_057264.3:n.563-37del
XM_011514051.1:c.161-37del	XP_011512353.1:n.161-37del
XM_011514052.1:c.563-37del	XP_011512354.1:n.563-37del
XR_925620.1:n.1380-37del
NM_016180.5:c.563-37del MANE Select	NP_057264.4:n.563-37del
NM_001012509.4:c.563-37del	NP_001012527.2:n.563-37del
NM_001297417.3:c.563-9549del	NP_001284346.2:n.563-9549del
NM_001297417.4:c.563-9549del	NP_001284346.2:n.563-9549del