Canonical Allele Identifier: CA443659221

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33951717T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951612T>C , CM000667.2:g.33951612T>C	GRCh38
NC_000005.9:g.33951717T>C , CM000667.1:g.33951717T>C	GRCh37
NC_000005.8:g.33987474T>C	NCBI36
NG_011691.2:g.38064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1098A>G MANE Select	ENSP00000296589.4:p.Gly366=
ENST00000296589.8:c.1098A>G	ENSP00000296589.4:p.Gly366=
ENST00000382102.7:c.1098A>G	ENSP00000371534.3:p.Gly366=
ENST00000509381.1:c.*40A>G	ENSP00000421100.1:n.*40A>G
ENST00000510600.1:c.573A>G	ENSP00000424010.1:p.Gly191=
NM_001012509.3:c.1098A>G	NP_001012527.1:p.Gly366=
NM_001297417.2:c.*40A>G	NP_001284346.2:n.*40A>G
NM_016180.4:c.1098A>G	NP_057264.3:p.Gly366=
XM_011514051.1:c.696A>G	XP_011512353.1:p.Gly232=
XR_925620.1:n.1915A>G
NM_016180.5:c.1098A>G MANE Select	NP_057264.4:p.Gly366=
NM_001012509.4:c.1098A>G	NP_001012527.2:p.Gly366=
NM_001297417.3:c.*40A>G	NP_001284346.2:n.*40A>G
NM_001297417.4:c.*40A>G	NP_001284346.2:n.*40A>G