Canonical Allele Identifier: CA443659216

Gene: SLC45A2

Linked Data

• MyVariant Identifiers: chr5:g.33951708A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951603A>T , CM000667.2:g.33951603A>T	GRCh38
NC_000005.9:g.33951708A>T , CM000667.1:g.33951708A>T	GRCh37
NC_000005.8:g.33987465A>T	NCBI36
NG_011691.2:g.38073T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1107T>A MANE Select	ENSP00000296589.4:p.Val369=
ENST00000296589.8:c.1107T>A	ENSP00000296589.4:p.Val369=
ENST00000382102.7:c.1107T>A	ENSP00000371534.3:p.Val369=
ENST00000509381.1:c.*49T>A	ENSP00000421100.1:n.*49T>A
ENST00000510600.1:c.582T>A	ENSP00000424010.1:p.Val194=
NM_001012509.3:c.1107T>A	NP_001012527.1:p.Val369=
NM_001297417.2:c.*49T>A	NP_001284346.2:n.*49T>A
NM_016180.4:c.1107T>A	NP_057264.3:p.Val369=
XM_011514051.1:c.705T>A	XP_011512353.1:p.Val235=
XR_925620.1:n.1924T>A
NM_016180.5:c.1107T>A MANE Select	NP_057264.4:p.Val369=
NM_001012509.4:c.1107T>A	NP_001012527.2:p.Val369=
NM_001297417.3:c.*49T>A	NP_001284346.2:n.*49T>A
NM_001297417.4:c.*49T>A	NP_001284346.2:n.*49T>A