Canonical Allele Identifier: CA1346967895
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129501T= , CM000665.2:g.14129501T= GRCh38
NC_000003.11:g.14171001T= , CM000665.1:g.14171001T= GRCh37
NC_000003.10:g.14146002T= NCBI36
NG_008975.1:g.9562T= , LRG_435:g.9562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*132T= ENSP00000395617.1:n.*132T=
ENST00000306077.5:c.102T= MANE Select ENSP00000303992.5:p.Gly34=
ENST00000306077.4:c.102T= ENSP00000303992.4:p.Gly34=
ENST00000432444.1:c.*132T= ENSP00000395617.1:n.*132T=
NM_024334.2:c.102T= , LRG_435t1:c.102T= NP_077310.1:p.Gly34=
XM_011534109.1:c.-4T= XP_011532411.1:n.-4T=
XM_017007176.2:c.-4T= XP_016862665.1:n.-4T=
NM_024334.3:c.102T= MANE Select NP_077310.1:p.Gly34=