Canonical Allele Identifier: CA3225596

Gene: SLC45A2

Linked Data

• ClinVar Variation Id: 773698
• ClinVar RCV Id: RCV000953505
• dbSNP Id: rs533984191
• ExAC: 5:33951771 G / A
• gnomAD v2: 5-33951771-G-A
• gnomAD v3: 5-33951666-G-A
• gnomAD v4: 5-33951666-G-A
• COSMIC: COSM3429390 ; COSM3429391
• MyVariant Identifiers: chr5:g.33951771G>A (hg19) ; chr5:g.33951666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951666G>A , CM000667.2:g.33951666G>A	GRCh38
NC_000005.9:g.33951771G>A , CM000667.1:g.33951771G>A	GRCh37
NC_000005.8:g.33987528G>A	NCBI36
NG_011691.2:g.38010C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1044C>T MANE Select	ENSP00000296589.4:p.Arg348=
ENST00000296589.8:c.1044C>T	ENSP00000296589.4:p.Arg348=
ENST00000382102.7:c.1044C>T	ENSP00000371534.3:p.Arg348=
ENST00000509381.1:c.718C>T	ENSP00000421100.1:p.Arg240Trp
ENST00000510600.1:c.519C>T	ENSP00000424010.1:p.Arg173=
NM_001012509.3:c.1044C>T	NP_001012527.1:p.Arg348=
NM_001297417.2:c.718C>T	NP_001284346.2:p.Arg240Trp
NM_016180.4:c.1044C>T	NP_057264.3:p.Arg348=
XM_011514051.1:c.642C>T	XP_011512353.1:p.Arg214=
XR_925620.1:n.1861C>T
NM_016180.5:c.1044C>T MANE Select	NP_057264.4:p.Arg348=
NM_001012509.4:c.1044C>T	NP_001012527.2:p.Arg348=
NM_001297417.3:c.718C>T	NP_001284346.2:p.Arg240Trp
NM_001297417.4:c.718C>T	NP_001284346.2:p.Arg240Trp