Canonical Allele Identifier: CA1346968551
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130816_14130817delinsTC , CM000665.2:g.14130816_14130817delinsTC GRCh38
NC_000003.11:g.14172316_14172317delinsTC , CM000665.1:g.14172316_14172317delinsTC GRCh37
NC_000003.10:g.14147317_14147318delinsTC NCBI36
NG_008975.1:g.10877_10878delinsTC , LRG_435:g.10877_10878delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*193-6_*193-5delinsTC ENSP00000395617.1:n.*193-6_*193-5delinsTC
ENST00000306077.5:c.163-6_163-5delinsTC MANE Select ENSP00000303992.5:n.163-6_163-5delinsTC
ENST00000306077.4:c.163-6_163-5delinsTC ENSP00000303992.4:n.163-6_163-5delinsTC
ENST00000432444.1:c.*193-6_*193-5delinsTC ENSP00000395617.1:n.*193-6_*193-5delinsTC
NM_024334.2:c.163-6_163-5delinsTC , LRG_435t1:c.163-6_163-5delinsTC NP_077310.1:n.163-6_163-5delinsTC
XM_011534109.1:c.58-6_58-5delinsTC XP_011532411.1:n.58-6_58-5delinsTC
XM_017007176.2:c.58-6_58-5delinsTC XP_016862665.1:n.58-6_58-5delinsTC
NM_024334.3:c.163-6_163-5delinsTC MANE Select NP_077310.1:n.163-6_163-5delinsTC