Canonical Allele Identifier: CA430367212

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190428353G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189563627G>T , CM000664.2:g.189563627G>T	GRCh38
NC_000002.11:g.190428353G>T , CM000664.1:g.190428353G>T	GRCh37
NC_000002.10:g.190136598G>T	NCBI36
NG_009027.1:g.22185C>A , LRG_837:g.22185C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.1359C>A MANE Select	ENSP00000261024.3:p.Ile453=
ENST00000261024.6:c.1359C>A	ENSP00000261024.2:p.Ile453=
NM_014585.5:c.1359C>A , LRG_837t1:c.1359C>A	NP_055400.1:p.Ile453=
XM_005246505.1:c.1239C>A	XP_005246562.1:p.Ile413=
XM_005246505.2:c.1239C>A	XP_005246562.1:p.Ile413=
XM_017003938.2:c.1239C>A	XP_016859427.1:p.Ile413=
NM_014585.6:c.1359C>A MANE Select	NP_055400.1:p.Ile453=