Canonical Allele Identifier: CA359389707

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33951676A>C (hg19) ; chr5:g.33951571A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951571A>C , CM000667.2:g.33951571A>C	GRCh38
NC_000005.9:g.33951676A>C , CM000667.1:g.33951676A>C	GRCh37
NC_000005.8:g.33987433A>C	NCBI36
NG_011691.2:g.38105T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1139T>G MANE Select	ENSP00000296589.4:p.Phe380Cys
ENST00000296589.8:c.1139T>G	ENSP00000296589.4:p.Phe380Cys
ENST00000382102.7:c.1139T>G	ENSP00000371534.3:p.Phe380Cys
ENST00000509381.1:c.*81T>G	ENSP00000421100.1:n.*81T>G
ENST00000510600.1:c.614T>G	ENSP00000424010.1:p.Phe205Cys
NM_001012509.3:c.1139T>G	NP_001012527.1:p.Phe380Cys
NM_001297417.2:c.*81T>G	NP_001284346.2:n.*81T>G
NM_016180.4:c.1139T>G	NP_057264.3:p.Phe380Cys
XM_011514051.1:c.737T>G	XP_011512353.1:p.Phe246Cys
XR_925620.1:n.1956T>G
NM_016180.5:c.1139T>G MANE Select	NP_057264.4:p.Phe380Cys
NM_001012509.4:c.1139T>G	NP_001012527.2:p.Phe380Cys
NM_001297417.3:c.*81T>G	NP_001284346.2:n.*81T>G
NM_001297417.4:c.*81T>G	NP_001284346.2:n.*81T>G