Canonical Allele Identifier: CA2664568570
Gene: TMEM43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129396_14129401del , CM000665.2:g.14129396_14129401del GRCh38
NC_000003.11:g.14170896_14170901del , CM000665.1:g.14170896_14170901del GRCh37
NC_000003.10:g.14145897_14145902del NCBI36
NG_008975.1:g.9457_9462del , LRG_435:g.9457_9462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*43-16_*43-11del ENSP00000395617.1:n.*43-16_*43-11del
ENST00000306077.5:c.13-16_13-11del MANE Select ENSP00000303992.5:n.13-16_13-11del
ENST00000306077.4:c.13-16_13-11del ENSP00000303992.4:n.13-16_13-11del
ENST00000432444.1:c.*43-16_*43-11del ENSP00000395617.1:n.*43-16_*43-11del
NM_024334.2:c.13-16_13-11del , LRG_435t1:c.13-16_13-11del NP_077310.1:n.13-16_13-11del
XM_011534109.1:c.-93-16_-93-11del XP_011532411.1:n.-93-16_-93-11del
XM_017007176.2:c.-93-16_-93-11del XP_016862665.1:n.-93-16_-93-11del
NM_024334.3:c.13-16_13-11del MANE Select NP_077310.1:n.13-16_13-11del