LDH info

Canonical Allele Identifier: CA271961
Gene: NIPBL HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 159031
ClinVar RCV Id: RCV000146516
dbSNP Id: rs587783882

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36976090C>T , CM000667.2:g.36976090C>T GRCh38
NC_000005.9:g.36976192C>T , CM000667.1:g.36976192C>T GRCh37
NC_000005.8:g.37011949C>T NCBI36
NG_006987.1:g.104208C>T
NG_006987.2:g.104208C>T

Transcript Alleles

HGVS Amino-acid change
NM_015384.4:c.1183C>T VV NP_056199.2:p.Gln395Ter
NM_133433.3:c.1183C>T VV NP_597677.2:p.Gln395Ter
XM_005248280.2:c.1183C>T XP_005248337.1:p.Gln395Ter
XM_005248282.3:c.439C>T XP_005248339.2:p.Gln147Ter
XM_006714467.2:c.1183C>T XP_006714530.1:p.Gln395Ter
XM_006714468.1:c.1183C>T XP_006714531.1:p.Gln395Ter
XM_011514014.1:c.1183C>T XP_011512316.1:p.Gln395Ter
XM_011514015.1:c.1183C>T XP_011512317.1:p.Gln395Ter
XM_005248280.3:c.1183C>T XP_005248337.1:p.Gln395Ter
XM_005248282.5:c.523C>T XP_005248339.3:p.Gln175Ter
XM_006714468.2:c.1183C>T XP_006714531.1:p.Gln395Ter
XM_017009329.1:c.1183C>T XP_016864818.1:p.Gln395Ter
XM_017009331.1:c.1183C>T XP_016864820.1:p.Gln395Ter
NM_133433.4:c.1183C>T VV MANE Preferred NP_597677.2:p.Gln395Ter
ENST00000282516.12:c.1183C>T ENSP00000282516.8:p.Gln395Ter
ENST00000448238.2:c.1183C>T ENSP00000406266.2:p.Gln395Ter
ENST00000504430.5:n.803C>T
ENST00000621733.1:c.1-88488C>T ENSP00000480694.1:p.=