Canonical Allele Identifier: CA430367490

Gene: SLC40A1

Linked Data

• dbSNP Id: rs1198028891
• gnomAD v2: 2-190439897-A-G
• gnomAD v4: 2-189575171-A-G
• MyVariant Identifiers: chr2:g.190439897A>G (hg19) ; chr2:g.189575171A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575171A>G , CM000664.2:g.189575171A>G	GRCh38
NC_000002.11:g.190439897A>G , CM000664.1:g.190439897A>G	GRCh37
NC_000002.10:g.190148142A>G	NCBI36
NG_009027.1:g.10641T>C , LRG_837:g.10641T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.261T>C MANE Select	ENSP00000261024.3:p.Ala87=
ENST00000261024.6:c.261T>C	ENSP00000261024.2:p.Ala87=
ENST00000418714.1:n.702T>C
ENST00000427241.5:c.261T>C	ENSP00000390005.1:p.Ala87=
ENST00000479598.5:n.542T>C
NM_014585.5:c.261T>C , LRG_837t1:c.261T>C	NP_055400.1:p.Ala87=
XM_005246505.1:c.141T>C	XP_005246562.1:p.Ala47=
XM_005246505.2:c.141T>C	XP_005246562.1:p.Ala47=
XM_017003938.2:c.141T>C	XP_016859427.1:p.Ala47=
NM_014585.6:c.261T>C MANE Select	NP_055400.1:p.Ala87=