Canonical Allele Identifier: CA1346967890
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129490G= , CM000665.2:g.14129490G= GRCh38
NC_000003.11:g.14170990G= , CM000665.1:g.14170990G= GRCh37
NC_000003.10:g.14145991G= NCBI36
NG_008975.1:g.9551G= , LRG_435:g.9551G=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*121G= ENSP00000395617.1:n.*121G=
ENST00000306077.5:c.91G= MANE Select ENSP00000303992.5:p.Glu31=
ENST00000306077.4:c.91G= ENSP00000303992.4:p.Glu31=
ENST00000432444.1:c.*121G= ENSP00000395617.1:n.*121G=
NM_024334.2:c.91G= , LRG_435t1:c.91G= NP_077310.1:p.Glu31=
XM_011534109.1:c.-15G= XP_011532411.1:n.-15G=
XM_017007176.2:c.-15G= XP_016862665.1:n.-15G=
NM_024334.3:c.91G= MANE Select NP_077310.1:p.Glu31=