Canonical Allele Identifier: CA1346967844
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129413A= , CM000665.2:g.14129413A= GRCh38
NC_000003.11:g.14170913A= , CM000665.1:g.14170913A= GRCh37
NC_000003.10:g.14145914A= NCBI36
NG_008975.1:g.9474A= , LRG_435:g.9474A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*44A= ENSP00000395617.1:n.*44A=
ENST00000306077.5:c.14A= MANE Select ENSP00000303992.5:p.Tyr5=
ENST00000306077.4:c.14A= ENSP00000303992.4:p.Tyr5=
ENST00000432444.1:c.*44A= ENSP00000395617.1:n.*44A=
NM_024334.2:c.14A= , LRG_435t1:c.14A= NP_077310.1:p.Tyr5=
XM_011534109.1:c.-92A= XP_011532411.1:n.-92A=
XM_017007176.2:c.-92A= XP_016862665.1:n.-92A=
NM_024334.3:c.14A= MANE Select NP_077310.1:p.Tyr5=