Canonical Allele Identifier: CA359389883

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33951720T>G (hg19) ; chr5:g.33951615T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951615T>G , CM000667.2:g.33951615T>G	GRCh38
NC_000005.9:g.33951720T>G , CM000667.1:g.33951720T>G	GRCh37
NC_000005.8:g.33987477T>G	NCBI36
NG_011691.2:g.38061A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1095A>C MANE Select	ENSP00000296589.4:p.Arg365Ser
ENST00000296589.8:c.1095A>C	ENSP00000296589.4:p.Arg365Ser
ENST00000382102.7:c.1095A>C	ENSP00000371534.3:p.Arg365Ser
ENST00000509381.1:c.*37A>C	ENSP00000421100.1:n.*37A>C
ENST00000510600.1:c.570A>C	ENSP00000424010.1:p.Arg190Ser
NM_001012509.3:c.1095A>C	NP_001012527.1:p.Arg365Ser
NM_001297417.2:c.*37A>C	NP_001284346.2:n.*37A>C
NM_016180.4:c.1095A>C	NP_057264.3:p.Arg365Ser
XM_011514051.1:c.693A>C	XP_011512353.1:p.Arg231Ser
XR_925620.1:n.1912A>C
NM_016180.5:c.1095A>C MANE Select	NP_057264.4:p.Arg365Ser
NM_001012509.4:c.1095A>C	NP_001012527.2:p.Arg365Ser
NM_001297417.3:c.*37A>C	NP_001284346.2:n.*37A>C
NM_001297417.4:c.*37A>C	NP_001284346.2:n.*37A>C