LDH info

Canonical Allele Identifier: CA4276978
Gene: ASL HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs769960006

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66086614C>T , CM000669.2:g.66086614C>T GRCh38
NC_000007.13:g.65551601C>T , CM000669.1:g.65551601C>T GRCh37
NC_000007.12:g.65189036C>T NCBI36
NG_009288.1:g.15826C>T

Transcript Alleles

HGVS Amino-acid change
NM_000048.3:c.476C>T VV NP_000039.2:p.Thr159Ile
NM_001024943.1:c.476C>T VV NP_001020114.1:p.Thr159Ile
NM_001024944.1:c.476C>T VV NP_001020115.1:p.Thr159Ile
NM_001024946.1:c.476C>T VV NP_001020117.1:p.Thr159Ile
NM_000048.4:c.476C>T VV MANE Preferred NP_000039.2:p.Thr159Ile
NM_001024943.2:c.476C>T VV NP_001020114.1:p.Thr159Ile
NM_001024944.2:c.476C>T VV NP_001020115.1:p.Thr159Ile
NM_001024946.2:c.476C>T VV NP_001020117.1:p.Thr159Ile
ENST00000304874.13:c.476C>T ENSP00000307188.9:p.Thr159Ile
ENST00000362000.9:c.281C>T ENSP00000354710.5:p.Thr94Ile
ENST00000380839.8:c.476C>T ENSP00000370219.4:p.Thr159Ile
ENST00000395331.3:c.476C>T ENSP00000378740.3:p.Thr159Ile
ENST00000395332.7:c.476C>T ENSP00000378741.3:p.Thr159Ile
ENST00000487982.5:n.542C>T