Canonical Allele Identifier: CA1346967927

Gene: TMEM43

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14129573G= , CM000665.2:g.14129573G=	GRCh38
NC_000003.11:g.14171073G= , CM000665.1:g.14171073G=	GRCh37
NC_000003.10:g.14146074G=	NCBI36
NG_008975.1:g.9634G= , LRG_435:g.9634G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*192+12G=	ENSP00000395617.1:n.*192+12G=
ENST00000306077.5:c.162+12G= MANE Select	ENSP00000303992.5:n.162+12G=
ENST00000306077.4:c.162+12G=	ENSP00000303992.4:n.162+12G=
ENST00000432444.1:c.*192+12G=	ENSP00000395617.1:n.*192+12G=
NM_024334.2:c.162+12G= , LRG_435t1:c.162+12G=	NP_077310.1:n.162+12G=
XM_011534109.1:c.57+12G=	XP_011532411.1:n.57+12G=
XM_017007176.2:c.57+12G=	XP_016862665.1:n.57+12G=
NM_024334.3:c.162+12G= MANE Select	NP_077310.1:n.162+12G=