Canonical Allele Identifier: CA1346965704
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125201C= , CM000665.2:g.14125201C= GRCh38
NC_000003.11:g.14166701C= , CM000665.1:g.14166701C= GRCh37
NC_000003.10:g.14141702C= NCBI36
NG_008975.1:g.5262C= , LRG_435:g.5262C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.8C= ENSP00000395617.1:p.Ala3=
ENST00000306077.5:c.8C= MANE Select ENSP00000303992.5:p.Ala3=
ENST00000306077.4:c.8C= ENSP00000303992.4:p.Ala3=
ENST00000432444.1:c.8C= ENSP00000395617.1:p.Ala3=
NM_024334.2:c.8C= , LRG_435t1:c.8C= NP_077310.1:p.Ala3=
XM_017007176.2:c.-329C= XP_016862665.1:n.-329C=
NM_024334.3:c.8C= MANE Select NP_077310.1:p.Ala3=