Canonical Allele Identifier: CA1315645109
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565585T= , CM000664.2:g.189565585T= GRCh38
NC_000002.11:g.190430311T= , CM000664.1:g.190430311T= GRCh37
NC_000002.10:g.190138556T= NCBI36
NG_009027.1:g.20227A= , LRG_837:g.20227A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.529A= MANE Select ENSP00000261024.3:p.Ile177=
ENST00000261024.6:c.529A= ENSP00000261024.2:p.Ile177=
ENST00000427241.5:c.529A= ENSP00000390005.1:p.Ile177=
NM_014585.5:c.529A= , LRG_837t1:c.529A= NP_055400.1:p.Ile177=
XM_005246505.1:c.409A= XP_005246562.1:p.Ile137=
XM_005246505.2:c.409A= XP_005246562.1:p.Ile137=
XM_017003938.2:c.409A= XP_016859427.1:p.Ile137=
NM_014585.6:c.529A= MANE Select NP_055400.1:p.Ile177=