Canonical Allele Identifier: CA349988695

Gene: SLC40A1

Linked Data

• dbSNP Id: rs1559011082
• MyVariant Identifiers: chr2:g.190430173G>T (hg19) ; chr2:g.189565447G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189565447G>T , CM000664.2:g.189565447G>T	GRCh38
NC_000002.11:g.190430173G>T , CM000664.1:g.190430173G>T	GRCh37
NC_000002.10:g.190138418G>T	NCBI36
NG_009027.1:g.20365C>A , LRG_837:g.20365C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.667C>A MANE Select	ENSP00000261024.3:p.Leu223Ile
ENST00000261024.6:c.667C>A	ENSP00000261024.2:p.Leu223Ile
NM_014585.5:c.667C>A , LRG_837t1:c.667C>A	NP_055400.1:p.Leu223Ile
XM_005246505.1:c.547C>A	XP_005246562.1:p.Leu183Ile
XM_005246505.2:c.547C>A	XP_005246562.1:p.Leu183Ile
XM_017003938.2:c.547C>A	XP_016859427.1:p.Leu183Ile
NM_014585.6:c.667C>A MANE Select	NP_055400.1:p.Leu223Ile