Canonical Allele Identifier: CA1346967842
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129410A= , CM000665.2:g.14129410A= GRCh38
NC_000003.11:g.14170910A= , CM000665.1:g.14170910A= GRCh37
NC_000003.10:g.14145911A= NCBI36
NG_008975.1:g.9471A= , LRG_435:g.9471A=

Transcript Alleles

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