Canonical Allele Identifier: CA2024142
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1092324
ClinVar RCV Id: RCV001412093
dbSNP Id: rs780756130
ExAC: 2:190428887 C / T
gnomAD v2: 2-190428887-C-T
gnomAD v3: 2-189564161-C-T
gnomAD v4: 2-189564161-C-T
MyVariant Identifiers: chr2:g.190428887C>T (hg19) chr2:g.189564161C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564161C>T , CM000664.2:g.189564161C>T GRCh38
NC_000002.11:g.190428887C>T , CM000664.1:g.190428887C>T GRCh37
NC_000002.10:g.190137132C>T NCBI36
NG_009027.1:g.21651G>A , LRG_837:g.21651G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.825G>A MANE Select ENSP00000261024.3:p.Glu275=
ENST00000261024.6:c.825G>A ENSP00000261024.2:p.Glu275=
NM_014585.5:c.825G>A , LRG_837t1:c.825G>A NP_055400.1:p.Glu275=
XM_005246505.1:c.705G>A XP_005246562.1:p.Glu235=
XM_005246505.2:c.705G>A XP_005246562.1:p.Glu235=
XM_017003938.2:c.705G>A XP_016859427.1:p.Glu235=
NM_014585.6:c.825G>A MANE Select NP_055400.1:p.Glu275=
Search 100 bp 5'
Search 100 bp 3'