Canonical Allele Identifier: CA180365344

Gene: TPD52

Linked Data

• dbSNP Id: rs1034354071
• gnomAD v3: 8-80037787-G-C
• gnomAD v4: 8-80037787-G-C
• MyVariant Identifiers: chr8:g.80950022G>C (hg19) ; chr8:g.80037787G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80037787G>C , CM000670.2:g.80037787G>C	GRCh38
NC_000008.10:g.80950022G>C , CM000670.1:g.80950022G>C	GRCh37
NC_000008.9:g.81112577G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518937.6:c.*329C>G MANE Select	ENSP00000429915.1:n.*329C>G
ENST00000379096.9:c.*329C>G	ENSP00000368390.4:n.*329C>G
ENST00000379097.7:c.*329C>G	ENSP00000368391.3:n.*329C>G
ENST00000448733.3:c.*329C>G	ENSP00000410222.2:n.*329C>G
ENST00000517427.5:c.*329C>G	ENSP00000429351.1:n.*329C>G
ENST00000517462.6:c.*687C>G	ENSP00000429708.1:n.*687C>G
ENST00000518937.5:c.*329C>G	ENSP00000429915.1:n.*329C>G
ENST00000519303.6:c.*329C>G	ENSP00000428951.1:n.*329C>G
ENST00000520527.5:c.*329C>G	ENSP00000429309.1:n.*329C>G
ENST00000522938.5:c.555+4833C>G	ENSP00000430858.2:n.555+4833C>G
ENST00000523193.5:n.831C>G
ENST00000523395.5:n.663C>G
NM_001025252.2:c.*329C>G	NP_001020423.1:n.*329C>G
NM_001025253.2:c.*329C>G	NP_001020424.1:n.*329C>G
NM_001287140.1:c.*329C>G	NP_001274069.1:n.*329C>G
NM_001287142.1:c.*329C>G	NP_001274071.1:n.*329C>G
NM_001287143.1:c.*329C>G	NP_001274072.1:n.*329C>G
NM_001287144.1:c.*439C>G	NP_001274073.1:n.*439C>G
NM_005079.3:c.*329C>G	NP_005070.1:n.*329C>G
NR_105033.1:n.1521C>G
NR_105034.1:n.984C>G
NR_105035.1:n.1170C>G
NR_105036.1:n.1114C>G
NR_105037.1:n.1115C>G
NM_001025252.3:c.*329C>G	NP_001020423.1:n.*329C>G
NM_001025253.3:c.*329C>G MANE Select	NP_001020424.1:n.*329C>G
NM_001287140.2:c.*329C>G	NP_001274069.1:n.*329C>G
NM_001287143.2:c.*329C>G	NP_001274072.1:n.*329C>G
NM_001287144.2:c.*439C>G	NP_001274073.1:n.*439C>G
NM_005079.4:c.*329C>G	NP_005070.1:n.*329C>G
NR_105033.2:n.1520C>G
NR_105034.2:n.889C>G
NR_105035.2:n.1075C>G
NR_105036.2:n.1035C>G
NR_105037.2:n.1036C>G
NM_001287142.2:c.*329C>G	NP_001274071.1:n.*329C>G
NM_001387778.1:c.435+4833C>G	NP_001374707.1:n.435+4833C>G
NM_001387779.1:c.436-3944C>G	NP_001374708.1:n.436-3944C>G
NM_001387780.1:c.460-3944C>G	NP_001374709.1:n.460-3944C>G
NR_170693.1:n.1024C>G
NR_170694.1:n.1051C>G