Canonical Allele Identifier: CA2662328891
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565207_189565216del , CM000664.2:g.189565207_189565216del GRCh38
NC_000002.11:g.190429933_190429942del , CM000664.1:g.190429933_190429942del GRCh37
NC_000002.10:g.190138178_190138187del NCBI36
NG_009027.1:g.20599_20608del , LRG_837:g.20599_20608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+141_760+150del MANE Select ENSP00000261024.3:n.760+141_760+150del
ENST00000261024.6:c.760+141_760+150del ENSP00000261024.2:n.760+141_760+150del
NM_014585.5:c.760+141_760+150del , LRG_837t1:c.760+141_760+150del NP_055400.1:n.760+141_760+150del
XM_005246505.1:c.640+141_640+150del XP_005246562.1:n.640+141_640+150del
XM_005246505.2:c.640+141_640+150del XP_005246562.1:n.640+141_640+150del
XM_017003938.2:c.640+141_640+150del XP_016859427.1:n.640+141_640+150del
NM_014585.6:c.760+141_760+150del MANE Select NP_055400.1:n.760+141_760+150del