LDH info

Canonical Allele Identifier: CA359504008
Gene: NIPBL HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36985864T>C , CM000667.2:g.36985864T>C GRCh38
NC_000005.9:g.36985966T>C , CM000667.1:g.36985966T>C GRCh37
NC_000005.8:g.37021723T>C NCBI36
NG_006987.1:g.113982T>C
NG_006987.2:g.113982T>C

Transcript Alleles

HGVS Amino-acid change
NM_015384.4:c.2684T>C VV NP_056199.2:p.Val895Ala
NM_133433.3:c.2684T>C VV NP_597677.2:p.Val895Ala
XM_005248280.2:c.2684T>C XP_005248337.1:p.Val895Ala
XM_005248282.3:c.1940T>C XP_005248339.2:p.Val647Ala
XM_006714467.2:c.2684T>C XP_006714530.1:p.Val895Ala
XM_006714468.1:c.2684T>C XP_006714531.1:p.Val895Ala
XM_011514014.1:c.2684T>C XP_011512316.1:p.Val895Ala
XM_011514015.1:c.2684T>C XP_011512317.1:p.Val895Ala
XM_005248280.3:c.2684T>C XP_005248337.1:p.Val895Ala
XM_005248282.5:c.2024T>C XP_005248339.3:p.Val675Ala
XM_006714468.2:c.2684T>C XP_006714531.1:p.Val895Ala
XM_017009329.1:c.2684T>C XP_016864818.1:p.Val895Ala
XM_017009330.2:c.1067T>C XP_016864819.1:p.Val356Ala
XM_017009331.1:c.1495+9462T>C XP_016864820.1:p.=
NM_133433.4:c.2684T>C VV MANE Preferred NP_597677.2:p.Val895Ala
NM_015384.5:c.2684T>C VV NP_056199.2:p.Val895Ala
ENST00000282516.12:c.2684T>C ENSP00000282516.8:p.Val895Ala
ENST00000448238.2:c.2684T>C ENSP00000406266.2:p.Val895Ala
ENST00000504430.5:n.2304T>C
ENST00000621733.1:c.1-78714T>C ENSP00000480694.1:p.=