Canonical Allele Identifier: CA1346965699
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125193C= , CM000665.2:g.14125193C= GRCh38
NC_000003.11:g.14166693C= , CM000665.1:g.14166693C= GRCh37
NC_000003.10:g.14141694C= NCBI36
NG_008975.1:g.5254C= , LRG_435:g.5254C=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.-1C= ENSP00000395617.1:n.-1C=
ENST00000306077.5:c.-1C= MANE Select ENSP00000303992.5:n.-1C=
ENST00000306077.4:c.-1C= ENSP00000303992.4:n.-1C=
ENST00000432444.1:c.-1C= ENSP00000395617.1:n.-1C=
NM_024334.2:c.-1C= , LRG_435t1:c.-1C= NP_077310.1:n.-1C=
XM_017007176.2:c.-337C= XP_016862665.1:n.-337C=
NM_024334.3:c.-1C= MANE Select NP_077310.1:n.-1C=