Canonical Allele Identifier: CA2755300757
Gene: TMEM43 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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