Canonical Allele Identifier: CA1346967855
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129431G= , CM000665.2:g.14129431G= GRCh38
NC_000003.11:g.14170931G= , CM000665.1:g.14170931G= GRCh37
NC_000003.10:g.14145932G= NCBI36
NG_008975.1:g.9492G= , LRG_435:g.9492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*62G= ENSP00000395617.1:n.*62G=
ENST00000306077.5:c.32G= MANE Select ENSP00000303992.5:p.Arg11=
ENST00000306077.4:c.32G= ENSP00000303992.4:p.Arg11=
ENST00000432444.1:c.*62G= ENSP00000395617.1:n.*62G=
NM_024334.2:c.32G= , LRG_435t1:c.32G= NP_077310.1:p.Arg11=
XM_011534109.1:c.-74G= XP_011532411.1:n.-74G=
XM_017007176.2:c.-74G= XP_016862665.1:n.-74G=
NM_024334.3:c.32G= MANE Select NP_077310.1:p.Arg11=