Canonical Allele Identifier: CA430502854
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190428950A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564224A>G , CM000664.2:g.189564224A>G GRCh38
NC_000002.11:g.190428950A>G , CM000664.1:g.190428950A>G GRCh37
NC_000002.10:g.190137195A>G NCBI36
NG_009027.1:g.21588T>C , LRG_837:g.21588T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.762T>C MANE Select ENSP00000261024.3:p.Asp254=
ENST00000261024.6:c.762T>C ENSP00000261024.2:p.Asp254=
NM_014585.5:c.762T>C , LRG_837t1:c.762T>C NP_055400.1:p.Asp254=
XM_005246505.1:c.642T>C XP_005246562.1:p.Asp214=
XM_005246505.2:c.642T>C XP_005246562.1:p.Asp214=
XM_017003938.2:c.642T>C XP_016859427.1:p.Asp214=
NM_014585.6:c.762T>C MANE Select NP_055400.1:p.Asp254=