Canonical Allele Identifier: CA349988082

Gene: SLC40A1

Linked Data

• COSMIC: COSM3990922
• MyVariant Identifiers: chr2:g.190428774C>G (hg19) ; chr2:g.189564048C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564048C>G , CM000664.2:g.189564048C>G	GRCh38
NC_000002.11:g.190428774C>G , CM000664.1:g.190428774C>G	GRCh37
NC_000002.10:g.190137019C>G	NCBI36
NG_009027.1:g.21764G>C , LRG_837:g.21764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.938G>C MANE Select	ENSP00000261024.3:p.Gly313Ala
ENST00000261024.6:c.938G>C	ENSP00000261024.2:p.Gly313Ala
NM_014585.5:c.938G>C , LRG_837t1:c.938G>C	NP_055400.1:p.Gly313Ala
XM_005246505.1:c.818G>C	XP_005246562.1:p.Gly273Ala
XM_005246505.2:c.818G>C	XP_005246562.1:p.Gly273Ala
XM_017003938.2:c.818G>C	XP_016859427.1:p.Gly273Ala
NM_014585.6:c.938G>C MANE Select	NP_055400.1:p.Gly313Ala