Canonical Allele Identifier: CA2664568714
Gene: TMEM43 HGNC NCBI

Linked Data

gnomAD v4: 3-14130724-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130724C>G , CM000665.2:g.14130724C>G GRCh38
NC_000003.11:g.14172224C>G , CM000665.1:g.14172224C>G GRCh37
NC_000003.10:g.14147225C>G NCBI36
NG_008975.1:g.10785C>G , LRG_435:g.10785C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*193-98C>G ENSP00000395617.1:n.*193-98C>G
ENST00000306077.5:c.163-98C>G MANE Select ENSP00000303992.5:n.163-98C>G
ENST00000306077.4:c.163-98C>G ENSP00000303992.4:n.163-98C>G
ENST00000432444.1:c.*193-98C>G ENSP00000395617.1:n.*193-98C>G
NM_024334.2:c.163-98C>G , LRG_435t1:c.163-98C>G NP_077310.1:n.163-98C>G
XM_011534109.1:c.58-98C>G XP_011532411.1:n.58-98C>G
XM_017007176.2:c.58-98C>G XP_016862665.1:n.58-98C>G
NM_024334.3:c.163-98C>G MANE Select NP_077310.1:n.163-98C>G