Canonical Allele Identifier: CA1346967835
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129393A= , CM000665.2:g.14129393A= GRCh38
NC_000003.11:g.14170893A= , CM000665.1:g.14170893A= GRCh37
NC_000003.10:g.14145894A= NCBI36
NG_008975.1:g.9454A= , LRG_435:g.9454A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*43-19A= ENSP00000395617.1:n.*43-19A=
ENST00000306077.5:c.13-19A= MANE Select ENSP00000303992.5:n.13-19A=
ENST00000306077.4:c.13-19A= ENSP00000303992.4:n.13-19A=
ENST00000432444.1:c.*43-19A= ENSP00000395617.1:n.*43-19A=
NM_024334.2:c.13-19A= , LRG_435t1:c.13-19A= NP_077310.1:n.13-19A=
XM_011534109.1:c.-93-19A= XP_011532411.1:n.-93-19A=
XM_017007176.2:c.-93-19A= XP_016862665.1:n.-93-19A=
NM_024334.3:c.13-19A= MANE Select NP_077310.1:n.13-19A=
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