Canonical Allele Identifier: CA1796805364

Gene: TPD52

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80119762_80119774delinsGTCCAGAAATAGA , CM000670.2:g.80119762_80119774delinsGTCCAGAAATAGA	GRCh38
NC_000008.10:g.81031997_81032009delinsGTCCAGAAATAGA , CM000670.1:g.81031997_81032009delinsGTCCAGAAATAGA	GRCh37
NC_000008.9:g.81194552_81194564delinsGTCCAGAAATAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518937.6:c.19+51651_19+51663delinsTCTATTTCTGGAC MANE Select	ENSP00000429915.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
ENST00000379096.9:c.19+51651_19+51663delinsTCTATTTCTGGAC	ENSP00000368390.4:n.19+51651_19+51663delinsTCTATTTCTGGAC
ENST00000518517.5:c.89+41_89+53delinsTCTATTTCTGGAC	ENSP00000430421.1:n.89+41_89+53delinsTCTATTTCTGGAC
ENST00000518937.5:c.19+51651_19+51663delinsTCTATTTCTGGAC	ENSP00000429915.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
ENST00000519250.5:n.236-55181_236-55169delinsTCTATTTCTGGAC
ENST00000519303.6:c.-423+51247_-423+51259delinsTCTATTTCTGGAC	ENSP00000428951.1:n.-423+51247_-423+51259delinsTCTATTTCTGGAC
ENST00000520795.5:c.177+51433_177+51445delinsTCTATTTCTGGAC
ENST00000521241.6:c.19+51651_19+51663delinsTCTATTTCTGGAC	ENSP00000430323.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
ENST00000521354.5:c.19+51651_19+51663delinsTCTATTTCTGGAC	ENSP00000430646.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
ENST00000521561.1:n.451+38663_451+38675delinsTCTATTTCTGGAC
ENST00000523753.5:c.89+41_89+53delinsTCTATTTCTGGAC	ENSP00000430140.1:n.89+41_89+53delinsTCTATTTCTGGAC
NM_001025253.2:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_001020424.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_001287144.1:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_001274073.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_005079.3:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_005070.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NR_105034.1:n.235+51651_235+51663delinsTCTATTTCTGGAC
NR_105035.1:n.305+41_305+53delinsTCTATTTCTGGAC
NR_105036.1:n.180+51247_180+51259delinsTCTATTTCTGGAC
NR_105037.1:n.250+41_250+53delinsTCTATTTCTGGAC
NM_001025253.3:c.19+51651_19+51663delinsTCTATTTCTGGAC MANE Select	NP_001020424.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_001287144.2:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_001274073.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_005079.4:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_005070.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NR_105034.2:n.140+51651_140+51663delinsTCTATTTCTGGAC
NR_105035.2:n.210+41_210+53delinsTCTATTTCTGGAC
NR_105036.2:n.101+51247_101+51259delinsTCTATTTCTGGAC
NR_105037.2:n.171+41_171+53delinsTCTATTTCTGGAC
NM_001387778.1:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_001374707.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_001387779.1:c.19+51651_19+51663delinsTCTATTTCTGGAC	NP_001374708.1:n.19+51651_19+51663delinsTCTATTTCTGGAC
NM_001387780.1:c.-65-9839_-65-9827delinsTCTATTTCTGGAC	NP_001374709.1:n.-65-9839_-65-9827delinsTCTATTTCTGGAC
NR_170693.1:n.140+51651_140+51663delinsTCTATTTCTGGAC
NR_170694.1:n.140+51651_140+51663delinsTCTATTTCTGGAC