Canonical Allele Identifier: CA1346973738
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141441A= , CM000665.2:g.14141441A= GRCh38
NC_000003.11:g.14182941A= , CM000665.1:g.14182941A= GRCh37
NC_000003.10:g.14157942A= NCBI36
NG_008975.1:g.21502A= , LRG_435:g.21502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*1031-152A= ENSP00000395617.1:n.*1031-152A=
ENST00000306077.5:c.1001-152A= MANE Select ENSP00000303992.5:n.1001-152A=
ENST00000306077.4:c.1001-152A= ENSP00000303992.4:n.1001-152A=
ENST00000601399.3:n.327+2144A=
ENST00000608606.1:c.236+2144A=
NM_024334.2:c.1001-152A= , LRG_435t1:c.1001-152A= NP_077310.1:n.1001-152A=
XM_011534109.1:c.896-152A= XP_011532411.1:n.896-152A=
XM_017007176.2:c.896-152A= XP_016862665.1:n.896-152A=
NM_024334.3:c.1001-152A= MANE Select NP_077310.1:n.1001-152A=