LDH info

Canonical Allele Identifier: CA12500638
Gene: NPY HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16476

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290600T>G , CM000669.2:g.24290600T>G GRCh38
NC_000007.13:g.24330219T>G , CM000669.1:g.24330219T>G GRCh37
NC_000007.12:g.24296744T>G NCBI36
NG_016148.1:g.11413T>G

Transcript Alleles

HGVS Amino-acid change
NM_000905.3:c.269+1021T>G VV NP_000896.1:p.=
XM_017012910.1:c.41+28757A>C XP_016868399.1:p.=
XM_017012911.1:c.41+28757A>C XP_016868400.1:p.=
XR_001745121.1:n.473+28757A>C
XR_001745122.1:n.345-93571A>C
XR_001745123.1:n.473+28757A>C
XR_001745124.1:n.473+28757A>C
XR_001745125.1:n.473+28757A>C
XR_001745126.1:n.473+28757A>C
XR_001745127.1:n.345-34901A>C
XR_001745129.1:n.473+28757A>C
XR_001745130.1:n.473+28757A>C
XR_001745131.1:n.473+28757A>C
XR_001745132.1:n.473+28757A>C
NM_000905.4:c.269+1021T>G VV MANE Preferred NP_000896.1:p.=
ENST00000242152.6:c.269+1021T>G ENSP00000242152.2:p.=
ENST00000405982.1:c.269+1021T>G ENSP00000385282.1:p.=
ENST00000407573.5:c.269+1021T>G ENSP00000384364.1:p.=