Canonical Allele Identifier: CA1315653851
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563647G= , CM000664.2:g.189563647G= GRCh38
NC_000002.11:g.190428373G= , CM000664.1:g.190428373G= GRCh37
NC_000002.10:g.190136618G= NCBI36
NG_009027.1:g.22165C= , LRG_837:g.22165C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1339C= MANE Select ENSP00000261024.3:p.Pro447=
ENST00000261024.6:c.1339C= ENSP00000261024.2:p.Pro447=
NM_014585.5:c.1339C= , LRG_837t1:c.1339C= NP_055400.1:p.Pro447=
XM_005246505.1:c.1219C= XP_005246562.1:p.Pro407=
XM_005246505.2:c.1219C= XP_005246562.1:p.Pro407=
XM_017003938.2:c.1219C= XP_016859427.1:p.Pro407=
NM_014585.6:c.1339C= MANE Select NP_055400.1:p.Pro447=