Canonical Allele Identifier: CA351534298

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14170981C>G (hg19) ; chr3:g.14129481C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14129481C>G , CM000665.2:g.14129481C>G	GRCh38
NC_000003.11:g.14170981C>G , CM000665.1:g.14170981C>G	GRCh37
NC_000003.10:g.14145982C>G	NCBI36
NG_008975.1:g.9542C>G , LRG_435:g.9542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*112C>G	ENSP00000395617.1:n.*112C>G
ENST00000306077.5:c.82C>G MANE Select	ENSP00000303992.5:p.Arg28Gly
ENST00000306077.4:c.82C>G	ENSP00000303992.4:p.Arg28Gly
ENST00000432444.1:c.*112C>G	ENSP00000395617.1:n.*112C>G
NM_024334.2:c.82C>G , LRG_435t1:c.82C>G	NP_077310.1:p.Arg28Gly
XM_011534109.1:c.-24C>G	XP_011532411.1:n.-24C>G
XM_017007176.2:c.-24C>G	XP_016862665.1:n.-24C>G
NM_024334.3:c.82C>G MANE Select	NP_077310.1:p.Arg28Gly