Canonical Allele Identifier: CA180365152
Gene: TPD52 HGNC NCBI

Linked Data

dbSNP Id: rs1049385723
gnomAD v4: 8-80037575-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80037575A>G , CM000670.2:g.80037575A>G GRCh38
NC_000008.10:g.80949810A>G , CM000670.1:g.80949810A>G GRCh37
NC_000008.9:g.81112365A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000518937.6:c.*541T>C MANE Select ENSP00000429915.1:n.*541T>C
ENST00000379096.9:c.*541T>C ENSP00000368390.4:n.*541T>C
ENST00000379097.7:c.*541T>C ENSP00000368391.3:n.*541T>C
ENST00000448733.3:c.*541T>C ENSP00000410222.2:n.*541T>C
ENST00000517427.5:c.*541T>C ENSP00000429351.1:n.*541T>C
ENST00000517462.6:c.*899T>C ENSP00000429708.1:n.*899T>C
ENST00000518937.5:c.*541T>C ENSP00000429915.1:n.*541T>C
ENST00000519303.6:c.*541T>C ENSP00000428951.1:n.*541T>C
ENST00000520527.5:c.*541T>C ENSP00000429309.1:n.*541T>C
ENST00000522938.5:c.555+5045T>C ENSP00000430858.2:n.555+5045T>C
NM_001025252.2:c.*541T>C NP_001020423.1:n.*541T>C
NM_001025253.2:c.*541T>C NP_001020424.1:n.*541T>C
NM_001287140.1:c.*541T>C NP_001274069.1:n.*541T>C
NM_001287142.1:c.*541T>C NP_001274071.1:n.*541T>C
NM_001287143.1:c.*541T>C NP_001274072.1:n.*541T>C
NM_001287144.1:c.*651T>C NP_001274073.1:n.*651T>C
NM_005079.3:c.*541T>C NP_005070.1:n.*541T>C
NR_105033.1:n.1733T>C
NR_105034.1:n.1196T>C
NR_105035.1:n.1382T>C
NR_105036.1:n.1326T>C
NR_105037.1:n.1327T>C
NM_001025252.3:c.*541T>C NP_001020423.1:n.*541T>C
NM_001025253.3:c.*541T>C MANE Select NP_001020424.1:n.*541T>C
NM_001287140.2:c.*541T>C NP_001274069.1:n.*541T>C
NM_001287143.2:c.*541T>C NP_001274072.1:n.*541T>C
NM_001287144.2:c.*651T>C NP_001274073.1:n.*651T>C
NM_005079.4:c.*541T>C NP_005070.1:n.*541T>C
NR_105033.2:n.1732T>C
NR_105034.2:n.1101T>C
NR_105035.2:n.1287T>C
NR_105036.2:n.1247T>C
NR_105037.2:n.1248T>C
NM_001287142.2:c.*541T>C NP_001274071.1:n.*541T>C
NM_001387778.1:c.435+5045T>C NP_001374707.1:n.435+5045T>C
NM_001387779.1:c.436-3732T>C NP_001374708.1:n.436-3732T>C
NM_001387780.1:c.460-3732T>C NP_001374709.1:n.460-3732T>C
NR_170693.1:n.1236T>C
NR_170694.1:n.1263T>C