LDH info

Canonical Allele Identifier: CA116361
Gene: SUFU HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 3569
ClinVar RCV Id: RCV000003750
dbSNP Id: rs28942088

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504196C>T , CM000672.2:g.102504196C>T GRCh38
NC_000010.10:g.104263953C>T , CM000672.1:g.104263953C>T GRCh37
NC_000010.9:g.104253943C>T NCBI36
NG_011901.1:g.3560G>A
NG_021338.1:g.5235C>T , LRG_521:g.5235C>T

Transcript Alleles

HGVS Amino-acid change
NM_001178133.1:c.44C>T VV NP_001171604.1:p.Pro15Leu
NM_016169.3:c.44C>T , LRG_521t1:c.44C>T NP_057253.2:p.Pro15Leu
XM_011539858.1:c.44C>T XP_011538160.1:p.Pro15Leu
XM_011539859.1:c.44C>T XP_011538161.1:p.Pro15Leu
XM_011539860.1:c.44C>T XP_011538162.1:p.Pro15Leu
XM_011539861.1:c.44C>T XP_011538163.1:p.Pro15Leu
XM_011539863.1:c.8+1210C>T XP_011538165.1:p.=
XM_011539864.1:c.44C>T XP_011538166.1:p.Pro15Leu
XM_011539858.3:c.44C>T XP_011538160.1:p.Pro15Leu
XM_011539860.3:c.44C>T XP_011538162.1:p.Pro15Leu
XM_011539861.3:c.44C>T XP_011538163.1:p.Pro15Leu
XM_011539863.3:c.8+1210C>T XP_011538165.1:p.=
XM_011539864.3:c.44C>T XP_011538166.1:p.Pro15Leu
NM_001178133.2:c.44C>T VV NP_001171604.1:p.Pro15Leu
NM_016169.4:c.44C>T VV NP_057253.2:p.Pro15Leu
ENST00000369899.6:c.44C>T ENSP00000358915.2:p.Pro15Leu
ENST00000369902.7:c.44C>T ENSP00000358918.3:p.Pro15Leu
ENST00000423559.2:c.44C>T ENSP00000411597.2:p.Pro15Leu