LDH info

Canonical Allele Identifier: CA123705
Gene: NTF4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14017
ClinVar RCV Id: RCV000015060
dbSNP Id: rs61732310

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061735G>A , CM000681.2:g.49061735G>A GRCh38
NC_000019.9:g.49564992G>A , CM000681.1:g.49564992G>A GRCh37
NC_000019.8:g.54256804G>A NCBI36
NG_016289.1:g.7133C>T

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.263C>T VV NP_006170.1:p.Ala88Val
XM_005258962.2:c.263C>T XP_005259019.1:p.Ala88Val
XM_006723232.2:c.263C>T XP_006723295.1:p.Ala88Val
XM_011527008.1:c.293C>T XP_011525310.1:p.Ala98Val
XM_011527009.1:c.263C>T XP_011525311.1:p.Ala88Val
XM_011527010.1:c.263C>T XP_011525312.1:p.Ala88Val
XM_005258962.3:c.263C>T XP_005259019.1:p.Ala88Val
XM_006723232.3:c.263C>T XP_006723295.1:p.Ala88Val
XM_011527008.2:c.293C>T XP_011525310.1:p.Ala98Val
XM_011527009.2:c.263C>T XP_011525311.1:p.Ala88Val
XM_011527010.2:c.263C>T XP_011525312.1:p.Ala88Val
XR_001753693.1:n.308C>T
XR_001753694.1:n.308C>T
ENST00000593537.1:n.263C>T ENSP00000469455.1:p.Ala88Val
ENST00000595857.5:c.263C>T ENSP00000471508.1:p.Ala88Val
ENST00000599795.5:c.243+20C>T ENSP00000470689.1:p.=