Canonical Allele Identifier: CA1315653802
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563603G= , CM000664.2:g.189563603G= GRCh38
NC_000002.11:g.190428329G= , CM000664.1:g.190428329G= GRCh37
NC_000002.10:g.190136574G= NCBI36
NG_009027.1:g.22209C= , LRG_837:g.22209C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1383C= MANE Select ENSP00000261024.3:p.Gly461=
ENST00000261024.6:c.1383C= ENSP00000261024.2:p.Gly461=
NM_014585.5:c.1383C= , LRG_837t1:c.1383C= NP_055400.1:p.Gly461=
XM_005246505.1:c.1263C= XP_005246562.1:p.Gly421=
XM_005246505.2:c.1263C= XP_005246562.1:p.Gly421=
XM_017003938.2:c.1263C= XP_016859427.1:p.Gly421=
NM_014585.6:c.1383C= MANE Select NP_055400.1:p.Gly461=