Canonical Allele Identifier: CA1346965705
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125202G= , CM000665.2:g.14125202G= GRCh38
NC_000003.11:g.14166702G= , CM000665.1:g.14166702G= GRCh37
NC_000003.10:g.14141703G= NCBI36
NG_008975.1:g.5263G= , LRG_435:g.5263G=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.9G= ENSP00000395617.1:p.Ala3=
ENST00000306077.5:c.9G= MANE Select ENSP00000303992.5:p.Ala3=
ENST00000306077.4:c.9G= ENSP00000303992.4:p.Ala3=
ENST00000432444.1:c.9G= ENSP00000395617.1:p.Ala3=
NM_024334.2:c.9G= , LRG_435t1:c.9G= NP_077310.1:p.Ala3=
XM_017007176.2:c.-328G= XP_016862665.1:n.-328G=
NM_024334.3:c.9G= MANE Select NP_077310.1:p.Ala3=