Canonical Allele Identifier: CA1346968558

Gene: TMEM43

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14130822G= , CM000665.2:g.14130822G=	GRCh38
NC_000003.11:g.14172322G= , CM000665.1:g.14172322G=	GRCh37
NC_000003.10:g.14147323G=	NCBI36
NG_008975.1:g.10883G= , LRG_435:g.10883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*193G=	ENSP00000395617.1:n.*193G=
ENST00000306077.5:c.163G= MANE Select	ENSP00000303992.5:p.Gly55=
ENST00000306077.4:c.163G=	ENSP00000303992.4:p.Gly55=
ENST00000432444.1:c.*193G=	ENSP00000395617.1:n.*193G=
NM_024334.2:c.163G= , LRG_435t1:c.163G=	NP_077310.1:p.Gly55=
XM_011534109.1:c.58G=	XP_011532411.1:p.Gly20=
XM_017007176.2:c.58G=	XP_016862665.1:p.Gly20=
NM_024334.3:c.163G= MANE Select	NP_077310.1:p.Gly55=