Canonical Allele Identifier: CA1346967904
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129516G= , CM000665.2:g.14129516G= GRCh38
NC_000003.11:g.14171016G= , CM000665.1:g.14171016G= GRCh37
NC_000003.10:g.14146017G= NCBI36
NG_008975.1:g.9577G= , LRG_435:g.9577G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*147G= ENSP00000395617.1:n.*147G=
ENST00000306077.5:c.117G= MANE Select ENSP00000303992.5:p.Gly39=
ENST00000306077.4:c.117G= ENSP00000303992.4:p.Gly39=
ENST00000432444.1:c.*147G= ENSP00000395617.1:n.*147G=
NM_024334.2:c.117G= , LRG_435t1:c.117G= NP_077310.1:p.Gly39=
XM_011534109.1:c.12G= XP_011532411.1:p.Gly4=
XM_017007176.2:c.12G= XP_016862665.1:p.Gly4=
NM_024334.3:c.117G= MANE Select NP_077310.1:p.Gly39=