Canonical Allele Identifier: CA3225602

Gene: SLC45A2

Linked Data

• ClinVar Variation Id: 2963397
• ClinVar RCV Id: RCV003823051
• dbSNP Id: rs11568736
• ExAC: 5:33951788 A / G
• gnomAD v2: 5-33951788-A-G
• gnomAD v3: 5-33951683-A-G
• gnomAD v4: 5-33951683-A-G
• MyVariant Identifiers: chr5:g.33951788A>G (hg19) ; chr5:g.33951683A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951683A>G , CM000667.2:g.33951683A>G	GRCh38
NC_000005.9:g.33951788A>G , CM000667.1:g.33951788A>G	GRCh37
NC_000005.8:g.33987545A>G	NCBI36
NG_011691.2:g.37993T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-6T>C MANE Select	ENSP00000296589.4:n.1033-6T>C
ENST00000296589.8:c.1033-6T>C	ENSP00000296589.4:n.1033-6T>C
ENST00000382102.7:c.1033-6T>C	ENSP00000371534.3:n.1033-6T>C
ENST00000509381.1:c.707-6T>C	ENSP00000421100.1:n.707-6T>C
ENST00000510600.1:c.508-6T>C	ENSP00000424010.1:n.508-6T>C
NM_001012509.3:c.1033-6T>C	NP_001012527.1:n.1033-6T>C
NM_001297417.2:c.707-6T>C	NP_001284346.2:n.707-6T>C
NM_016180.4:c.1033-6T>C	NP_057264.3:n.1033-6T>C
XM_011514051.1:c.631-6T>C	XP_011512353.1:n.631-6T>C
XR_925620.1:n.1850-6T>C
NM_016180.5:c.1033-6T>C MANE Select	NP_057264.4:n.1033-6T>C
NM_001012509.4:c.1033-6T>C	NP_001012527.2:n.1033-6T>C
NM_001297417.3:c.707-6T>C	NP_001284346.2:n.707-6T>C
NM_001297417.4:c.707-6T>C	NP_001284346.2:n.707-6T>C