Canonical Allele Identifier: CA1346967893
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129498G= , CM000665.2:g.14129498G= GRCh38
NC_000003.11:g.14170998G= , CM000665.1:g.14170998G= GRCh37
NC_000003.10:g.14145999G= NCBI36
NG_008975.1:g.9559G= , LRG_435:g.9559G=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*129G= ENSP00000395617.1:n.*129G=
ENST00000306077.5:c.99G= MANE Select ENSP00000303992.5:p.Ser33=
ENST00000306077.4:c.99G= ENSP00000303992.4:p.Ser33=
ENST00000432444.1:c.*129G= ENSP00000395617.1:n.*129G=
NM_024334.2:c.99G= , LRG_435t1:c.99G= NP_077310.1:p.Ser33=
XM_011534109.1:c.-7G= XP_011532411.1:n.-7G=
XM_017007176.2:c.-7G= XP_016862665.1:n.-7G=
NM_024334.3:c.99G= MANE Select NP_077310.1:p.Ser33=