Canonical Allele Identifier: CA349987365
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563707T>A , CM000664.2:g.189563707T>A GRCh38
NC_000002.11:g.190428433T>A , CM000664.1:g.190428433T>A GRCh37
NC_000002.10:g.190136678T>A NCBI36
NG_009027.1:g.22105A>T , LRG_837:g.22105A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1279A>T MANE Select ENSP00000261024.3:p.Thr427Ser
ENST00000261024.6:c.1279A>T ENSP00000261024.2:p.Thr427Ser
NM_014585.5:c.1279A>T , LRG_837t1:c.1279A>T NP_055400.1:p.Thr427Ser
XM_005246505.1:c.1159A>T XP_005246562.1:p.Thr387Ser
XM_005246505.2:c.1159A>T XP_005246562.1:p.Thr387Ser
XM_017003938.2:c.1159A>T XP_016859427.1:p.Thr387Ser
NM_014585.6:c.1279A>T MANE Select NP_055400.1:p.Thr427Ser