Canonical Allele Identifier: CA1346968499
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130731A= , CM000665.2:g.14130731A= GRCh38
NC_000003.11:g.14172231A= , CM000665.1:g.14172231A= GRCh37
NC_000003.10:g.14147232A= NCBI36
NG_008975.1:g.10792A= , LRG_435:g.10792A=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*193-91A= ENSP00000395617.1:n.*193-91A=
ENST00000306077.5:c.163-91A= MANE Select ENSP00000303992.5:n.163-91A=
ENST00000306077.4:c.163-91A= ENSP00000303992.4:n.163-91A=
ENST00000432444.1:c.*193-91A= ENSP00000395617.1:n.*193-91A=
NM_024334.2:c.163-91A= , LRG_435t1:c.163-91A= NP_077310.1:n.163-91A=
XM_011534109.1:c.58-91A= XP_011532411.1:n.58-91A=
XM_017007176.2:c.58-91A= XP_016862665.1:n.58-91A=
NM_024334.3:c.163-91A= MANE Select NP_077310.1:n.163-91A=
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