Canonical Allele Identifier: CA349987429

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190428464C>A (hg19) ; chr2:g.189563738C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189563738C>A , CM000664.2:g.189563738C>A	GRCh38
NC_000002.11:g.190428464C>A , CM000664.1:g.190428464C>A	GRCh37
NC_000002.10:g.190136709C>A	NCBI36
NG_009027.1:g.22074G>T , LRG_837:g.22074G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.1248G>T MANE Select	ENSP00000261024.3:p.Glu416Asp
ENST00000261024.6:c.1248G>T	ENSP00000261024.2:p.Glu416Asp
NM_014585.5:c.1248G>T , LRG_837t1:c.1248G>T	NP_055400.1:p.Glu416Asp
XM_005246505.1:c.1128G>T	XP_005246562.1:p.Glu376Asp
XM_005246505.2:c.1128G>T	XP_005246562.1:p.Glu376Asp
XM_017003938.2:c.1128G>T	XP_016859427.1:p.Glu376Asp
NM_014585.6:c.1248G>T MANE Select	NP_055400.1:p.Glu416Asp