Canonical Allele Identifier: CA62902882

Gene: SLC40A1

Linked Data

• dbSNP Id: rs1030564012
• gnomAD v3: 2-189563653-T-C
• gnomAD v4: 2-189563653-T-C
• MyVariant Identifiers: chr2:g.190428379T>C (hg19) ; chr2:g.189563653T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189563653T>C , CM000664.2:g.189563653T>C	GRCh38
NC_000002.11:g.190428379T>C , CM000664.1:g.190428379T>C	GRCh37
NC_000002.10:g.190136624T>C	NCBI36
NG_009027.1:g.22159A>G , LRG_837:g.22159A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.1333A>G MANE Select	ENSP00000261024.3:p.Thr445Ala
ENST00000261024.6:c.1333A>G	ENSP00000261024.2:p.Thr445Ala
NM_014585.5:c.1333A>G , LRG_837t1:c.1333A>G	NP_055400.1:p.Thr445Ala
XM_005246505.1:c.1213A>G	XP_005246562.1:p.Thr405Ala
XM_005246505.2:c.1213A>G	XP_005246562.1:p.Thr405Ala
XM_017003938.2:c.1213A>G	XP_016859427.1:p.Thr405Ala
NM_014585.6:c.1333A>G MANE Select	NP_055400.1:p.Thr445Ala