Canonical Allele Identifier: CA351536243
Gene: TMEM43 HGNC NCBI

Linked Data

gnomAD v4: 3-14139257-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14139257C>A , CM000665.2:g.14139257C>A GRCh38
NC_000003.11:g.14180757C>A , CM000665.1:g.14180757C>A GRCh37
NC_000003.10:g.14155758C>A NCBI36
NG_008975.1:g.19318C>A , LRG_435:g.19318C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*990C>A ENSP00000395617.1:n.*990C>A
ENST00000306077.5:c.960C>A MANE Select ENSP00000303992.5:p.Phe320Leu
ENST00000306077.4:c.960C>A ENSP00000303992.4:p.Phe320Leu
ENST00000601399.3:n.287C>A
ENST00000608606.1:c.196C>A
NM_024334.2:c.960C>A , LRG_435t1:c.960C>A NP_077310.1:p.Phe320Leu
XM_011534109.1:c.855C>A XP_011532411.1:p.Phe285Leu
XM_017007176.2:c.855C>A XP_016862665.1:p.Phe285Leu
NM_024334.3:c.960C>A MANE Select NP_077310.1:p.Phe320Leu