Canonical Allele Identifier: CA1796774778

Gene: TPD52

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80037622C= , CM000670.2:g.80037622C=	GRCh38
NC_000008.10:g.80949857C= , CM000670.1:g.80949857C=	GRCh37
NC_000008.9:g.81112412C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518937.6:c.*494G= MANE Select	ENSP00000429915.1:n.*494G=
ENST00000379096.9:c.*494G=	ENSP00000368390.4:n.*494G=
ENST00000379097.7:c.*494G=	ENSP00000368391.3:n.*494G=
ENST00000448733.3:c.*494G=	ENSP00000410222.2:n.*494G=
ENST00000517427.5:c.*494G=	ENSP00000429351.1:n.*494G=
ENST00000517462.6:c.*852G=	ENSP00000429708.1:n.*852G=
ENST00000518937.5:c.*494G=	ENSP00000429915.1:n.*494G=
ENST00000519303.6:c.*494G=	ENSP00000428951.1:n.*494G=
ENST00000520527.5:c.*494G=	ENSP00000429309.1:n.*494G=
ENST00000522938.5:c.555+4998G=	ENSP00000430858.2:n.555+4998G=
NM_001025252.2:c.*494G=	NP_001020423.1:n.*494G=
NM_001025253.2:c.*494G=	NP_001020424.1:n.*494G=
NM_001287140.1:c.*494G=	NP_001274069.1:n.*494G=
NM_001287142.1:c.*494G=	NP_001274071.1:n.*494G=
NM_001287143.1:c.*494G=	NP_001274072.1:n.*494G=
NM_001287144.1:c.*604G=	NP_001274073.1:n.*604G=
NM_005079.3:c.*494G=	NP_005070.1:n.*494G=
NR_105033.1:n.1686G=
NR_105034.1:n.1149G=
NR_105035.1:n.1335G=
NR_105036.1:n.1279G=
NR_105037.1:n.1280G=
NM_001025252.3:c.*494G=	NP_001020423.1:n.*494G=
NM_001025253.3:c.*494G= MANE Select	NP_001020424.1:n.*494G=
NM_001287140.2:c.*494G=	NP_001274069.1:n.*494G=
NM_001287143.2:c.*494G=	NP_001274072.1:n.*494G=
NM_001287144.2:c.*604G=	NP_001274073.1:n.*604G=
NM_005079.4:c.*494G=	NP_005070.1:n.*494G=
NR_105033.2:n.1685G=
NR_105034.2:n.1054G=
NR_105035.2:n.1240G=
NR_105036.2:n.1200G=
NR_105037.2:n.1201G=
NM_001287142.2:c.*494G=	NP_001274071.1:n.*494G=
NM_001387778.1:c.435+4998G=	NP_001374707.1:n.435+4998G=
NM_001387779.1:c.436-3779G=	NP_001374708.1:n.436-3779G=
NM_001387780.1:c.460-3779G=	NP_001374709.1:n.460-3779G=
NR_170693.1:n.1189G=
NR_170694.1:n.1216G=