Canonical Allele Identifier: CA430503063
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190428731G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564005G>T , CM000664.2:g.189564005G>T GRCh38
NC_000002.11:g.190428731G>T , CM000664.1:g.190428731G>T GRCh37
NC_000002.10:g.190136976G>T NCBI36
NG_009027.1:g.21807C>A , LRG_837:g.21807C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.981C>A MANE Select ENSP00000261024.3:p.Ile327=
ENST00000261024.6:c.981C>A ENSP00000261024.2:p.Ile327=
NM_014585.5:c.981C>A , LRG_837t1:c.981C>A NP_055400.1:p.Ile327=
XM_005246505.1:c.861C>A XP_005246562.1:p.Ile287=
XM_005246505.2:c.861C>A XP_005246562.1:p.Ile287=
XM_017003938.2:c.861C>A XP_016859427.1:p.Ile287=
NM_014585.6:c.981C>A MANE Select NP_055400.1:p.Ile327=
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