Canonical Allele Identifier: CA2504363776
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564251_189564254del , CM000664.2:g.189564251_189564254del GRCh38
NC_000002.11:g.190428977_190428980del , CM000664.1:g.190428977_190428980del GRCh37
NC_000002.10:g.190137222_190137225del NCBI36
NG_009027.1:g.21560_21563del , LRG_837:g.21560_21563del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.761-27_761-24del MANE Select ENSP00000261024.3:n.761-27_761-24del
ENST00000261024.6:c.761-27_761-24del ENSP00000261024.2:n.761-27_761-24del
NM_014585.5:c.761-27_761-24del , LRG_837t1:c.761-27_761-24del NP_055400.1:n.761-27_761-24del
XM_005246505.1:c.641-27_641-24del XP_005246562.1:n.641-27_641-24del
XM_005246505.2:c.641-27_641-24del XP_005246562.1:n.641-27_641-24del
XM_017003938.2:c.641-27_641-24del XP_016859427.1:n.641-27_641-24del
NM_014585.6:c.761-27_761-24del MANE Select NP_055400.1:n.761-27_761-24del