Canonical Allele Identifier: CA430367179
Gene: SLC40A1 HGNC NCBI

Linked Data

COSMIC: COSM5614990
MyVariant Identifiers: chr2:g.190428311G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563585G>T , CM000664.2:g.189563585G>T GRCh38
NC_000002.11:g.190428311G>T , CM000664.1:g.190428311G>T GRCh37
NC_000002.10:g.190136556G>T NCBI36
NG_009027.1:g.22227C>A , LRG_837:g.22227C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1401C>A MANE Select ENSP00000261024.3:p.Ile467=
ENST00000261024.6:c.1401C>A ENSP00000261024.2:p.Ile467=
NM_014585.5:c.1401C>A , LRG_837t1:c.1401C>A NP_055400.1:p.Ile467=
XM_005246505.1:c.1281C>A XP_005246562.1:p.Ile427=
XM_005246505.2:c.1281C>A XP_005246562.1:p.Ile427=
XM_017003938.2:c.1281C>A XP_016859427.1:p.Ile427=
NM_014585.6:c.1401C>A MANE Select NP_055400.1:p.Ile467=
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