Canonical Allele Identifier: CA1346967838
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129399_14129400delinsTC , CM000665.2:g.14129399_14129400delinsTC GRCh38
NC_000003.11:g.14170899_14170900delinsTC , CM000665.1:g.14170899_14170900delinsTC GRCh37
NC_000003.10:g.14145900_14145901delinsTC NCBI36
NG_008975.1:g.9460_9461delinsTC , LRG_435:g.9460_9461delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*43-13_*43-12delinsTC ENSP00000395617.1:n.*43-13_*43-12delinsTC
ENST00000306077.5:c.13-13_13-12delinsTC MANE Select ENSP00000303992.5:n.13-13_13-12delinsTC
ENST00000306077.4:c.13-13_13-12delinsTC ENSP00000303992.4:n.13-13_13-12delinsTC
ENST00000432444.1:c.*43-13_*43-12delinsTC ENSP00000395617.1:n.*43-13_*43-12delinsTC
NM_024334.2:c.13-13_13-12delinsTC , LRG_435t1:c.13-13_13-12delinsTC NP_077310.1:n.13-13_13-12delinsTC
XM_011534109.1:c.-93-13_-93-12delinsTC XP_011532411.1:n.-93-13_-93-12delinsTC
XM_017007176.2:c.-93-13_-93-12delinsTC XP_016862665.1:n.-93-13_-93-12delinsTC
NM_024334.3:c.13-13_13-12delinsTC MANE Select NP_077310.1:n.13-13_13-12delinsTC