Canonical Allele Identifier: CA1346967891
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129495C= , CM000665.2:g.14129495C= GRCh38
NC_000003.11:g.14170995C= , CM000665.1:g.14170995C= GRCh37
NC_000003.10:g.14145996C= NCBI36
NG_008975.1:g.9556C= , LRG_435:g.9556C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*126C= ENSP00000395617.1:n.*126C=
ENST00000306077.5:c.96C= MANE Select ENSP00000303992.5:p.Thr32=
ENST00000306077.4:c.96C= ENSP00000303992.4:p.Thr32=
ENST00000432444.1:c.*126C= ENSP00000395617.1:n.*126C=
NM_024334.2:c.96C= , LRG_435t1:c.96C= NP_077310.1:p.Thr32=
XM_011534109.1:c.-10C= XP_011532411.1:n.-10C=
XM_017007176.2:c.-10C= XP_016862665.1:n.-10C=
NM_024334.3:c.96C= MANE Select NP_077310.1:p.Thr32=