Canonical Allele Identifier: CA1346965698
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125192C= , CM000665.2:g.14125192C= GRCh38
NC_000003.11:g.14166692C= , CM000665.1:g.14166692C= GRCh37
NC_000003.10:g.14141693C= NCBI36
NG_008975.1:g.5253C= , LRG_435:g.5253C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.-2C= ENSP00000395617.1:n.-2C=
ENST00000306077.5:c.-2C= MANE Select ENSP00000303992.5:n.-2C=
ENST00000306077.4:c.-2C= ENSP00000303992.4:n.-2C=
ENST00000432444.1:c.-2C= ENSP00000395617.1:n.-2C=
NM_024334.2:c.-2C= , LRG_435t1:c.-2C= NP_077310.1:n.-2C=
XM_017007176.2:c.-338C= XP_016862665.1:n.-338C=
NM_024334.3:c.-2C= MANE Select NP_077310.1:n.-2C=