Canonical Allele Identifier: CA1346967918

Gene: TMEM43

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14129552C= , CM000665.2:g.14129552C=	GRCh38
NC_000003.11:g.14171052C= , CM000665.1:g.14171052C=	GRCh37
NC_000003.10:g.14146053C=	NCBI36
NG_008975.1:g.9613C= , LRG_435:g.9613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*183C=	ENSP00000395617.1:n.*183C=
ENST00000306077.5:c.153C= MANE Select	ENSP00000303992.5:p.Phe51=
ENST00000306077.4:c.153C=	ENSP00000303992.4:p.Phe51=
ENST00000432444.1:c.*183C=	ENSP00000395617.1:n.*183C=
NM_024334.2:c.153C= , LRG_435t1:c.153C=	NP_077310.1:p.Phe51=
XM_011534109.1:c.48C=	XP_011532411.1:p.Phe16=
XM_017007176.2:c.48C=	XP_016862665.1:p.Phe16=
NM_024334.3:c.153C= MANE Select	NP_077310.1:p.Phe51=