Canonical Allele Identifier: CA2553788924
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575314del , CM000664.2:g.189575314del GRCh38
NC_000002.11:g.190440040del , CM000664.1:g.190440040del GRCh37
NC_000002.10:g.190148285del NCBI36
NG_009027.1:g.10498del , LRG_837:g.10498del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.118del MANE Select ENSP00000261024.3:p.Arg40GlyfsTer12
ENST00000261024.6:c.118del ENSP00000261024.2:p.Arg40GlyfsTer12
ENST00000418714.1:n.559del
ENST00000427241.5:c.118del ENSP00000390005.1:p.Arg40GlyfsTer12
ENST00000455320.5:c.118del ENSP00000413549.1:p.Arg40GlyfsTer12
ENST00000479598.5:n.399del
NM_014585.5:c.118del , LRG_837t1:c.118del NP_055400.1:p.Arg40GlyfsTer12
XM_005246505.1:c.-3del XP_005246562.1:n.-3del
XM_005246505.2:c.-3del XP_005246562.1:n.-3del
XM_017003938.2:c.-3del XP_016859427.1:n.-3del
NM_014585.6:c.118del MANE Select NP_055400.1:p.Arg40GlyfsTer12