Canonical Allele Identifier: CA1315654462
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564170G= , CM000664.2:g.189564170G= GRCh38
NC_000002.11:g.190428896G= , CM000664.1:g.190428896G= GRCh37
NC_000002.10:g.190137141G= NCBI36
NG_009027.1:g.21642C= , LRG_837:g.21642C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.816C= MANE Select ENSP00000261024.3:p.Asn272=
ENST00000261024.6:c.816C= ENSP00000261024.2:p.Asn272=
NM_014585.5:c.816C= , LRG_837t1:c.816C= NP_055400.1:p.Asn272=
XM_005246505.1:c.696C= XP_005246562.1:p.Asn232=
XM_005246505.2:c.696C= XP_005246562.1:p.Asn232=
XM_017003938.2:c.696C= XP_016859427.1:p.Asn232=
NM_014585.6:c.816C= MANE Select NP_055400.1:p.Asn272=