Canonical Allele Identifier: CA1315655588
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565245_189565246delinsGC , CM000664.2:g.189565245_189565246delinsGC GRCh38
NC_000002.11:g.190429971_190429972delinsGC , CM000664.1:g.190429971_190429972delinsGC GRCh37
NC_000002.10:g.190138216_190138217delinsGC NCBI36
NG_009027.1:g.20566_20567delinsGC , LRG_837:g.20566_20567delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+108_760+109delinsGC MANE Select ENSP00000261024.3:n.760+108_760+109delinsGC
ENST00000261024.6:c.760+108_760+109delinsGC ENSP00000261024.2:n.760+108_760+109delinsGC
NM_014585.5:c.760+108_760+109delinsGC , LRG_837t1:c.760+108_760+109delinsGC NP_055400.1:n.760+108_760+109delinsGC
XM_005246505.1:c.640+108_640+109delinsGC XP_005246562.1:n.640+108_640+109delinsGC
XM_005246505.2:c.640+108_640+109delinsGC XP_005246562.1:n.640+108_640+109delinsGC
XM_017003938.2:c.640+108_640+109delinsGC XP_016859427.1:n.640+108_640+109delinsGC
NM_014585.6:c.760+108_760+109delinsGC MANE Select NP_055400.1:n.760+108_760+109delinsGC