Canonical Allele Identifier: CA349988240

Gene: SLC40A1

Linked Data

• dbSNP Id: rs2030850100
• MyVariant Identifiers: chr2:g.190428846G>T (hg19) ; chr2:g.189564120G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564120G>T , CM000664.2:g.189564120G>T	GRCh38
NC_000002.11:g.190428846G>T , CM000664.1:g.190428846G>T	GRCh37
NC_000002.10:g.190137091G>T	NCBI36
NG_009027.1:g.21692C>A , LRG_837:g.21692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.866C>A MANE Select	ENSP00000261024.3:p.Ala289Asp
ENST00000261024.6:c.866C>A	ENSP00000261024.2:p.Ala289Asp
NM_014585.5:c.866C>A , LRG_837t1:c.866C>A	NP_055400.1:p.Ala289Asp
XM_005246505.1:c.746C>A	XP_005246562.1:p.Ala249Asp
XM_005246505.2:c.746C>A	XP_005246562.1:p.Ala249Asp
XM_017003938.2:c.746C>A	XP_016859427.1:p.Ala249Asp
NM_014585.6:c.866C>A MANE Select	NP_055400.1:p.Ala289Asp