LDH info

Canonical Allele Identifier: CA16340294
Gene: TPD52 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10957961

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80119587A>G , CM000670.2:g.80119587A>G GRCh38
NC_000008.10:g.81031822A>G , CM000670.1:g.81031822A>G GRCh37
NC_000008.9:g.81194377A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001025253.2:c.19+51838T>C VV NP_001020424.1:p.=
NM_001287144.1:c.19+51838T>C VV NP_001274073.1:p.=
NM_005079.3:c.19+51838T>C VV NP_005070.1:p.=
NR_105034.1:n.235+51838T>C
NR_105035.1:n.305+228T>C
NR_105036.1:n.180+51434T>C
NR_105037.1:n.250+228T>C
NM_001025253.3:c.19+51838T>C VV NP_001020424.1:p.=
NM_001287144.2:c.19+51838T>C VV NP_001274073.1:p.=
NM_005079.4:c.19+51838T>C VV NP_005070.1:p.=
NR_105034.2:n.140+51838T>C
NR_105035.2:n.210+228T>C
NR_105036.2:n.101+51434T>C
NR_105037.2:n.171+228T>C
NM_001387778.1:c.19+51838T>C VV NP_001374707.1:p.=
NM_001387779.1:c.19+51838T>C VV NP_001374708.1:p.=
NM_001387780.1:c.-65-9652T>C VV NP_001374709.1:p.=
NR_170693.1:n.140+51838T>C
NR_170694.1:n.140+51838T>C
ENST00000379096.9:c.19+51838T>C ENSP00000368390.4:p.=
ENST00000518517.5:c.89+228T>C ENSP00000430421.1:p.=
ENST00000518937.5:c.19+51838T>C ENSP00000429915.1:p.=
ENST00000519250.5:n.236-54994T>C
ENST00000519303.6:c.-423+51434T>C ENSP00000428951.1:p.=
ENST00000520795.5:n.177+51620T>C
ENST00000521241.6:c.19+51838T>C ENSP00000430323.1:p.=
ENST00000521354.5:c.19+51838T>C ENSP00000430646.1:p.=
ENST00000521561.1:n.451+38850T>C
ENST00000523753.5:c.89+228T>C ENSP00000430140.1:p.=