Canonical Allele Identifier: CA1346973825
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141623T= , CM000665.2:g.14141623T= GRCh38
NC_000003.11:g.14183123T= , CM000665.1:g.14183123T= GRCh37
NC_000003.10:g.14158124T= NCBI36
NG_008975.1:g.21684T= , LRG_435:g.21684T=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1061T= ENSP00000395617.1:n.*1061T=
ENST00000306077.5:c.1031T= MANE Select ENSP00000303992.5:p.Val344=
ENST00000306077.4:c.1031T= ENSP00000303992.4:p.Val344=
ENST00000601399.3:n.327+2326T=
ENST00000608606.1:c.236+2326T=
NM_024334.2:c.1031T= , LRG_435t1:c.1031T= NP_077310.1:p.Val344=
XM_011534109.1:c.926T= XP_011532411.1:p.Val309=
XM_017007176.2:c.926T= XP_016862665.1:p.Val309=
NM_024334.3:c.1031T= MANE Select NP_077310.1:p.Val344=