Canonical Allele Identifier: CA338162240

Gene: SLC45A1

Linked Data

• MyVariant Identifiers: chr1:g.8385917A>T (hg19) ; chr1:g.8325857A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8325857A>T , CM000663.2:g.8325857A>T	GRCh38
NC_000001.10:g.8385917A>T , CM000663.1:g.8385917A>T	GRCh37
NC_000001.9:g.8308504A>T	NCBI36
NG_034025.1:g.12773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471889.7:c.530A>T MANE Select	ENSP00000418096.3:p.Asp177Val
ENST00000289877.8:c.530A>T	ENSP00000289877.8:p.Asp177Val
ENST00000471889.5:c.632A>T	ENSP00000418096.2:p.Asp211Val
NM_001080397.2:c.632A>T	NP_001073866.2:p.Asp211Val
XM_011541530.1:c.632A>T	XP_011539832.1:p.Asp211Val
XM_011541531.1:c.539A>T	XP_011539833.1:p.Asp180Val
XM_011541530.2:c.632A>T	XP_011539832.1:p.Asp211Val
XM_011541531.2:c.539A>T	XP_011539833.1:p.Asp180Val
XM_024447371.1:c.539A>T	XP_024303139.1:p.Asp180Val
XM_024447372.1:c.-77A>T	XP_024303140.1:n.-77A>T
NM_001080397.3:c.530A>T MANE Select	NP_001073866.3:p.Asp177Val
NM_001379614.1:c.530A>T	NP_001366543.1:p.Asp177Val
NM_001379615.1:c.437A>T	NP_001366544.1:p.Asp146Val
NM_001379616.1:c.437A>T	NP_001366545.1:p.Asp146Val
NM_001379617.1:c.-77A>T	NP_001366546.1:n.-77A>T
NM_001379618.1:c.-77A>T	NP_001366547.1:n.-77A>T