Canonical Allele Identifier: CA1346965636
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125092C= , CM000665.2:g.14125092C= GRCh38
NC_000003.11:g.14166592C= , CM000665.1:g.14166592C= GRCh37
NC_000003.10:g.14141593C= NCBI36
NG_008975.1:g.5153C= , LRG_435:g.5153C=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.-102C= ENSP00000395617.1:n.-102C=
ENST00000306077.5:c.-102C= MANE Select ENSP00000303992.5:n.-102C=
ENST00000306077.4:c.-102C= ENSP00000303992.4:n.-102C=
ENST00000432444.1:c.-102C= ENSP00000395617.1:n.-102C=
NM_024334.2:c.-102C= , LRG_435t1:c.-102C= NP_077310.1:n.-102C=
XM_017007176.2:c.-438C= XP_016862665.1:n.-438C=
NM_024334.3:c.-102C= MANE Select NP_077310.1:n.-102C=
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