Canonical Allele Identifier: CA2687711080

Gene: TPD52

Linked Data

• gnomAD v4: 8-80037749-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80037749G>T , CM000670.2:g.80037749G>T	GRCh38
NC_000008.10:g.80949984G>T , CM000670.1:g.80949984G>T	GRCh37
NC_000008.9:g.81112539G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518937.6:c.*367C>A MANE Select	ENSP00000429915.1:n.*367C>A
ENST00000379096.9:c.*367C>A	ENSP00000368390.4:n.*367C>A
ENST00000379097.7:c.*367C>A	ENSP00000368391.3:n.*367C>A
ENST00000448733.3:c.*367C>A	ENSP00000410222.2:n.*367C>A
ENST00000517427.5:c.*367C>A	ENSP00000429351.1:n.*367C>A
ENST00000517462.6:c.*725C>A	ENSP00000429708.1:n.*725C>A
ENST00000518937.5:c.*367C>A	ENSP00000429915.1:n.*367C>A
ENST00000519303.6:c.*367C>A	ENSP00000428951.1:n.*367C>A
ENST00000520527.5:c.*367C>A	ENSP00000429309.1:n.*367C>A
ENST00000522938.5:c.555+4871C>A	ENSP00000430858.2:n.555+4871C>A
ENST00000523193.5:n.869C>A
ENST00000523395.5:n.701C>A
NM_001025252.2:c.*367C>A	NP_001020423.1:n.*367C>A
NM_001025253.2:c.*367C>A	NP_001020424.1:n.*367C>A
NM_001287140.1:c.*367C>A	NP_001274069.1:n.*367C>A
NM_001287142.1:c.*367C>A	NP_001274071.1:n.*367C>A
NM_001287143.1:c.*367C>A	NP_001274072.1:n.*367C>A
NM_001287144.1:c.*477C>A	NP_001274073.1:n.*477C>A
NM_005079.3:c.*367C>A	NP_005070.1:n.*367C>A
NR_105033.1:n.1559C>A
NR_105034.1:n.1022C>A
NR_105035.1:n.1208C>A
NR_105036.1:n.1152C>A
NR_105037.1:n.1153C>A
NM_001025252.3:c.*367C>A	NP_001020423.1:n.*367C>A
NM_001025253.3:c.*367C>A MANE Select	NP_001020424.1:n.*367C>A
NM_001287140.2:c.*367C>A	NP_001274069.1:n.*367C>A
NM_001287143.2:c.*367C>A	NP_001274072.1:n.*367C>A
NM_001287144.2:c.*477C>A	NP_001274073.1:n.*477C>A
NM_005079.4:c.*367C>A	NP_005070.1:n.*367C>A
NR_105033.2:n.1558C>A
NR_105034.2:n.927C>A
NR_105035.2:n.1113C>A
NR_105036.2:n.1073C>A
NR_105037.2:n.1074C>A
NM_001287142.2:c.*367C>A	NP_001274071.1:n.*367C>A
NM_001387778.1:c.435+4871C>A	NP_001374707.1:n.435+4871C>A
NM_001387779.1:c.436-3906C>A	NP_001374708.1:n.436-3906C>A
NM_001387780.1:c.460-3906C>A	NP_001374709.1:n.460-3906C>A
NR_170693.1:n.1062C>A
NR_170694.1:n.1089C>A