Canonical Allele Identifier: CA1796805180

Gene: TPD52

Linked Data

• dbSNP Id: rs1808100477

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80119521G>C , CM000670.2:g.80119521G>C	GRCh38
NC_000008.10:g.81031756G>C , CM000670.1:g.81031756G>C	GRCh37
NC_000008.9:g.81194311G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518937.6:c.19+51904C>G MANE Select	ENSP00000429915.1:n.19+51904C>G
ENST00000379096.9:c.19+51904C>G	ENSP00000368390.4:n.19+51904C>G
ENST00000518517.5:c.89+294C>G	ENSP00000430421.1:n.89+294C>G
ENST00000518937.5:c.19+51904C>G	ENSP00000429915.1:n.19+51904C>G
ENST00000519250.5:n.236-54928C>G
ENST00000519303.6:c.-423+51500C>G	ENSP00000428951.1:n.-423+51500C>G
ENST00000520795.5:c.177+51686C>G
ENST00000521241.6:c.19+51904C>G	ENSP00000430323.1:n.19+51904C>G
ENST00000521354.5:c.19+51904C>G	ENSP00000430646.1:n.19+51904C>G
ENST00000521561.1:n.451+38916C>G
ENST00000523753.5:c.89+294C>G	ENSP00000430140.1:n.89+294C>G
NM_001025253.2:c.19+51904C>G	NP_001020424.1:n.19+51904C>G
NM_001287144.1:c.19+51904C>G	NP_001274073.1:n.19+51904C>G
NM_005079.3:c.19+51904C>G	NP_005070.1:n.19+51904C>G
NR_105034.1:n.235+51904C>G
NR_105035.1:n.305+294C>G
NR_105036.1:n.180+51500C>G
NR_105037.1:n.250+294C>G
NM_001025253.3:c.19+51904C>G MANE Select	NP_001020424.1:n.19+51904C>G
NM_001287144.2:c.19+51904C>G	NP_001274073.1:n.19+51904C>G
NM_005079.4:c.19+51904C>G	NP_005070.1:n.19+51904C>G
NR_105034.2:n.140+51904C>G
NR_105035.2:n.210+294C>G
NR_105036.2:n.101+51500C>G
NR_105037.2:n.171+294C>G
NM_001387778.1:c.19+51904C>G	NP_001374707.1:n.19+51904C>G
NM_001387779.1:c.19+51904C>G	NP_001374708.1:n.19+51904C>G
NM_001387780.1:c.-65-9586C>G	NP_001374709.1:n.-65-9586C>G
NR_170693.1:n.140+51904C>G
NR_170694.1:n.140+51904C>G