Canonical Allele Identifier: CA1346965642
Gene: TMEM43 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125102G= , CM000665.2:g.14125102G= GRCh38
NC_000003.11:g.14166602G= , CM000665.1:g.14166602G= GRCh37
NC_000003.10:g.14141603G= NCBI36
NG_008975.1:g.5163G= , LRG_435:g.5163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.-92G= ENSP00000395617.1:n.-92G=
ENST00000306077.5:c.-92G= MANE Select ENSP00000303992.5:n.-92G=
ENST00000306077.4:c.-92G= ENSP00000303992.4:n.-92G=
ENST00000432444.1:c.-92G= ENSP00000395617.1:n.-92G=
NM_024334.2:c.-92G= , LRG_435t1:c.-92G= NP_077310.1:n.-92G=
XM_017007176.2:c.-428G= XP_016862665.1:n.-428G=
NM_024334.3:c.-92G= MANE Select NP_077310.1:n.-92G=
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