Canonical Allele Identifier: CA1315653770
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563557A= , CM000664.2:g.189563557A= GRCh38
NC_000002.11:g.190428283A= , CM000664.1:g.190428283A= GRCh37
NC_000002.10:g.190136528A= NCBI36
NG_009027.1:g.22255T= , LRG_837:g.22255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+27T= MANE Select ENSP00000261024.3:n.1402+27T=
ENST00000261024.6:c.1402+27T= ENSP00000261024.2:n.1402+27T=
NM_014585.5:c.1402+27T= , LRG_837t1:c.1402+27T= NP_055400.1:n.1402+27T=
XM_005246505.1:c.1282+27T= XP_005246562.1:n.1282+27T=
XM_005246505.2:c.1282+27T= XP_005246562.1:n.1282+27T=
XM_017003938.2:c.1282+27T= XP_016859427.1:n.1282+27T=
NM_014585.6:c.1402+27T= MANE Select NP_055400.1:n.1402+27T=