LDH info

Canonical Allele Identifier: CA4277390
Gene: ASL HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs749788626

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66092848C>T , CM000669.2:g.66092848C>T GRCh38
NC_000007.13:g.65557835C>T , CM000669.1:g.65557835C>T GRCh37
NC_000007.12:g.65195270C>T NCBI36
NG_009288.1:g.22060C>T

Transcript Alleles

HGVS Amino-acid change
NM_000048.3:c.1331C>T VV NP_000039.2:p.Ala444Val
NM_001024943.1:c.1331C>T VV NP_001020114.1:p.Ala444Val
NM_001024944.1:c.1271C>T VV NP_001020115.1:p.Ala424Val
NM_001024946.1:c.1253C>T VV NP_001020117.1:p.Ala418Val
NM_000048.4:c.1331C>T VV MANE Preferred NP_000039.2:p.Ala444Val
NM_001024943.2:c.1331C>T VV NP_001020114.1:p.Ala444Val
NM_001024944.2:c.1271C>T VV NP_001020115.1:p.Ala424Val
NM_001024946.2:c.1253C>T VV NP_001020117.1:p.Ala418Val
ENST00000304874.13:c.1331C>T ENSP00000307188.9:p.Ala444Val
ENST00000380839.8:c.1253C>T ENSP00000370219.4:p.Ala418Val
ENST00000395331.3:c.1271C>T ENSP00000378740.3:p.Ala424Val
ENST00000395332.7:c.1331C>T ENSP00000378741.3:p.Ala444Val
ENST00000450043.2:n.563+185C>T ENSP00000396527.2:p.=
ENST00000464970.1:n.534C>T
ENST00000488343.1:n.148-56C>T
ENST00000493708.5:n.812C>T