Canonical Allele Identifier: CA349988395
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs1263004397

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564187C>G , CM000664.2:g.189564187C>G GRCh38
NC_000002.11:g.190428913C>G , CM000664.1:g.190428913C>G GRCh37
NC_000002.10:g.190137158C>G NCBI36
NG_009027.1:g.21625G>C , LRG_837:g.21625G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.799G>C MANE Select ENSP00000261024.3:p.Gly267Arg
ENST00000261024.6:c.799G>C ENSP00000261024.2:p.Gly267Arg
NM_014585.5:c.799G>C , LRG_837t1:c.799G>C NP_055400.1:p.Gly267Arg
XM_005246505.1:c.679G>C XP_005246562.1:p.Gly227Arg
XM_005246505.2:c.679G>C XP_005246562.1:p.Gly227Arg
XM_017003938.2:c.679G>C XP_016859427.1:p.Gly227Arg
NM_014585.6:c.799G>C MANE Select NP_055400.1:p.Gly267Arg