Canonical Allele Identifier: CA1346968498
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130729G= , CM000665.2:g.14130729G= GRCh38
NC_000003.11:g.14172229G= , CM000665.1:g.14172229G= GRCh37
NC_000003.10:g.14147230G= NCBI36
NG_008975.1:g.10790G= , LRG_435:g.10790G=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*193-93G= ENSP00000395617.1:n.*193-93G=
ENST00000306077.5:c.163-93G= MANE Select ENSP00000303992.5:n.163-93G=
ENST00000306077.4:c.163-93G= ENSP00000303992.4:n.163-93G=
ENST00000432444.1:c.*193-93G= ENSP00000395617.1:n.*193-93G=
NM_024334.2:c.163-93G= , LRG_435t1:c.163-93G= NP_077310.1:n.163-93G=
XM_011534109.1:c.58-93G= XP_011532411.1:n.58-93G=
XM_017007176.2:c.58-93G= XP_016862665.1:n.58-93G=
NM_024334.3:c.163-93G= MANE Select NP_077310.1:n.163-93G=
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