Canonical Allele Identifier: CA2662328564
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563544_189563561del , CM000664.2:g.189563544_189563561del GRCh38
NC_000002.11:g.190428270_190428287del , CM000664.1:g.190428270_190428287del GRCh37
NC_000002.10:g.190136515_190136532del NCBI36
NG_009027.1:g.22253_22270del , LRG_837:g.22253_22270del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+25_1402+42del MANE Select ENSP00000261024.3:n.1402+25_1402+42del
ENST00000261024.6:c.1402+25_1402+42del ENSP00000261024.2:n.1402+25_1402+42del
NM_014585.5:c.1402+25_1402+42del , LRG_837t1:c.1402+25_1402+42del NP_055400.1:n.1402+25_1402+42del
XM_005246505.1:c.1282+25_1282+42del XP_005246562.1:n.1282+25_1282+42del
XM_005246505.2:c.1282+25_1282+42del XP_005246562.1:n.1282+25_1282+42del
XM_017003938.2:c.1282+25_1282+42del XP_016859427.1:n.1282+25_1282+42del
NM_014585.6:c.1402+25_1402+42del MANE Select NP_055400.1:n.1402+25_1402+42del