Canonical Allele Identifier: CA2662328936
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565245G>A , CM000664.2:g.189565245G>A GRCh38
NC_000002.11:g.190429971G>A , CM000664.1:g.190429971G>A GRCh37
NC_000002.10:g.190138216G>A NCBI36
NG_009027.1:g.20567C>T , LRG_837:g.20567C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+109C>T MANE Select ENSP00000261024.3:n.760+109C>T
ENST00000261024.6:c.760+109C>T ENSP00000261024.2:n.760+109C>T
NM_014585.5:c.760+109C>T , LRG_837t1:c.760+109C>T NP_055400.1:n.760+109C>T
XM_005246505.1:c.640+109C>T XP_005246562.1:n.640+109C>T
XM_005246505.2:c.640+109C>T XP_005246562.1:n.640+109C>T
XM_017003938.2:c.640+109C>T XP_016859427.1:n.640+109C>T
NM_014585.6:c.760+109C>T MANE Select NP_055400.1:n.760+109C>T