Canonical Allele Identifier: CA2687711052
Gene: TPD52 HGNC NCBI

Linked Data

gnomAD v4: 8-80037643-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80037643G>A , CM000670.2:g.80037643G>A GRCh38
NC_000008.10:g.80949878G>A , CM000670.1:g.80949878G>A GRCh37
NC_000008.9:g.81112433G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518937.6:c.*473C>T MANE Select ENSP00000429915.1:n.*473C>T
ENST00000379096.9:c.*473C>T ENSP00000368390.4:n.*473C>T
ENST00000379097.7:c.*473C>T ENSP00000368391.3:n.*473C>T
ENST00000448733.3:c.*473C>T ENSP00000410222.2:n.*473C>T
ENST00000517427.5:c.*473C>T ENSP00000429351.1:n.*473C>T
ENST00000517462.6:c.*831C>T ENSP00000429708.1:n.*831C>T
ENST00000518937.5:c.*473C>T ENSP00000429915.1:n.*473C>T
ENST00000519303.6:c.*473C>T ENSP00000428951.1:n.*473C>T
ENST00000520527.5:c.*473C>T ENSP00000429309.1:n.*473C>T
ENST00000522938.5:c.555+4977C>T ENSP00000430858.2:n.555+4977C>T
NM_001025252.2:c.*473C>T NP_001020423.1:n.*473C>T
NM_001025253.2:c.*473C>T NP_001020424.1:n.*473C>T
NM_001287140.1:c.*473C>T NP_001274069.1:n.*473C>T
NM_001287142.1:c.*473C>T NP_001274071.1:n.*473C>T
NM_001287143.1:c.*473C>T NP_001274072.1:n.*473C>T
NM_001287144.1:c.*583C>T NP_001274073.1:n.*583C>T
NM_005079.3:c.*473C>T NP_005070.1:n.*473C>T
NR_105033.1:n.1665C>T
NR_105034.1:n.1128C>T
NR_105035.1:n.1314C>T
NR_105036.1:n.1258C>T
NR_105037.1:n.1259C>T
NM_001025252.3:c.*473C>T NP_001020423.1:n.*473C>T
NM_001025253.3:c.*473C>T MANE Select NP_001020424.1:n.*473C>T
NM_001287140.2:c.*473C>T NP_001274069.1:n.*473C>T
NM_001287143.2:c.*473C>T NP_001274072.1:n.*473C>T
NM_001287144.2:c.*583C>T NP_001274073.1:n.*583C>T
NM_005079.4:c.*473C>T NP_005070.1:n.*473C>T
NR_105033.2:n.1664C>T
NR_105034.2:n.1033C>T
NR_105035.2:n.1219C>T
NR_105036.2:n.1179C>T
NR_105037.2:n.1180C>T
NM_001287142.2:c.*473C>T NP_001274071.1:n.*473C>T
NM_001387778.1:c.435+4977C>T NP_001374707.1:n.435+4977C>T
NM_001387779.1:c.436-3800C>T NP_001374708.1:n.436-3800C>T
NM_001387780.1:c.460-3800C>T NP_001374709.1:n.460-3800C>T
NR_170693.1:n.1168C>T
NR_170694.1:n.1195C>T