Canonical Allele Identifier: CA1315653679
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575197T= , CM000664.2:g.189575197T= GRCh38
NC_000002.11:g.190439923T= , CM000664.1:g.190439923T= GRCh37
NC_000002.10:g.190148168T= NCBI36
NG_009027.1:g.10615A= , LRG_837:g.10615A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.235A= MANE Select ENSP00000261024.3:p.Ile79=
ENST00000261024.6:c.235A= ENSP00000261024.2:p.Ile79=
ENST00000418714.1:n.676A=
ENST00000427241.5:c.235A= ENSP00000390005.1:p.Ile79=
ENST00000479598.5:n.516A=
NM_014585.5:c.235A= , LRG_837t1:c.235A= NP_055400.1:p.Ile79=
XM_005246505.1:c.115A= XP_005246562.1:p.Ile39=
XM_005246505.2:c.115A= XP_005246562.1:p.Ile39=
XM_017003938.2:c.115A= XP_016859427.1:p.Ile39=
NM_014585.6:c.235A= MANE Select NP_055400.1:p.Ile79=