Canonical Allele Identifier: CA1315654296
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564018C= , CM000664.2:g.189564018C= GRCh38
NC_000002.11:g.190428744C= , CM000664.1:g.190428744C= GRCh37
NC_000002.10:g.190136989C= NCBI36
NG_009027.1:g.21794G= , LRG_837:g.21794G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.968G= MANE Select ENSP00000261024.3:p.Gly323=
ENST00000261024.6:c.968G= ENSP00000261024.2:p.Gly323=
NM_014585.5:c.968G= , LRG_837t1:c.968G= NP_055400.1:p.Gly323=
XM_005246505.1:c.848G= XP_005246562.1:p.Gly283=
XM_005246505.2:c.848G= XP_005246562.1:p.Gly283=
XM_017003938.2:c.848G= XP_016859427.1:p.Gly283=
NM_014585.6:c.968G= MANE Select NP_055400.1:p.Gly323=