Canonical Allele Identifier: CA1346965703
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125199C= , CM000665.2:g.14125199C= GRCh38
NC_000003.11:g.14166699C= , CM000665.1:g.14166699C= GRCh37
NC_000003.10:g.14141700C= NCBI36
NG_008975.1:g.5260C= , LRG_435:g.5260C=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.6C= ENSP00000395617.1:p.Ala2=
ENST00000306077.5:c.6C= MANE Select ENSP00000303992.5:p.Ala2=
ENST00000306077.4:c.6C= ENSP00000303992.4:p.Ala2=
ENST00000432444.1:c.6C= ENSP00000395617.1:p.Ala2=
NM_024334.2:c.6C= , LRG_435t1:c.6C= NP_077310.1:p.Ala2=
XM_017007176.2:c.-331C= XP_016862665.1:n.-331C=
NM_024334.3:c.6C= MANE Select NP_077310.1:p.Ala2=