Canonical Allele Identifier: CA1346967892
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129497C= , CM000665.2:g.14129497C= GRCh38
NC_000003.11:g.14170997C= , CM000665.1:g.14170997C= GRCh37
NC_000003.10:g.14145998C= NCBI36
NG_008975.1:g.9558C= , LRG_435:g.9558C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*128C= ENSP00000395617.1:n.*128C=
ENST00000306077.5:c.98C= MANE Select ENSP00000303992.5:p.Ser33=
ENST00000306077.4:c.98C= ENSP00000303992.4:p.Ser33=
ENST00000432444.1:c.*128C= ENSP00000395617.1:n.*128C=
NM_024334.2:c.98C= , LRG_435t1:c.98C= NP_077310.1:p.Ser33=
XM_011534109.1:c.-8C= XP_011532411.1:n.-8C=
XM_017007176.2:c.-8C= XP_016862665.1:n.-8C=
NM_024334.3:c.98C= MANE Select NP_077310.1:p.Ser33=