Canonical Allele Identifier: CA559293845

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1424904169
• gnomAD v2: 5-33963770-G-A
• gnomAD v4: 5-33963665-G-A
• MyVariant Identifiers: chr5:g.33963770G>A (hg19) ; chr5:g.33963665G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963665G>A , CM000667.2:g.33963665G>A	GRCh38
NC_000005.9:g.33963770G>A , CM000667.1:g.33963770G>A	GRCh37
NC_000005.8:g.33999527G>A	NCBI36
NG_011691.2:g.26011C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296589.9:c.888+26C>T MANE Select	ENSP00000296589.4:n.888+26C>T
ENST00000296589.8:c.888+26C>T	ENSP00000296589.4:n.888+26C>T
ENST00000382102.7:c.888+26C>T	ENSP00000371534.3:n.888+26C>T
ENST00000505056.1:n.716C>T
ENST00000509381.1:c.563-9161C>T	ENSP00000421100.1:n.563-9161C>T
ENST00000510600.1:c.363+26C>T	ENSP00000424010.1:n.363+26C>T
NM_001012509.3:c.888+26C>T	NP_001012527.1:n.888+26C>T
NM_001297417.2:c.563-9161C>T	NP_001284346.2:n.563-9161C>T
NM_016180.4:c.888+26C>T	NP_057264.3:n.888+26C>T
XM_011514051.1:c.486+26C>T	XP_011512353.1:n.486+26C>T
XM_011514052.1:c.888+26C>T	XP_011512354.1:n.888+26C>T
XR_925620.1:n.1705+26C>T
NM_016180.5:c.888+26C>T MANE Select	NP_057264.4:n.888+26C>T
NM_001012509.4:c.888+26C>T	NP_001012527.2:n.888+26C>T
NM_001297417.3:c.563-9161C>T	NP_001284346.2:n.563-9161C>T
NM_001297417.4:c.563-9161C>T	NP_001284346.2:n.563-9161C>T