LDH info

Canonical Allele Identifier: CA4566152
Gene: AOC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs45558339

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150857907G>A , CM000669.2:g.150857907G>A GRCh38
NC_000007.13:g.150554995G>A , CM000669.1:g.150554995G>A GRCh37
NC_000007.12:g.150185928G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001091.3:c.1437G>A VV NP_001082.2:p.Met479Ile
NM_001272072.1:c.1437G>A VV NP_001259001.1:p.Met479Ile
XM_011516008.1:c.1437G>A XP_011514310.1:p.Met479Ile
XM_011516009.1:c.1437G>A XP_011514311.1:p.Met479Ile
XR_928169.1:n.296-16462C>T
XR_928170.1:n.425+10709C>T
XR_928171.1:n.298-16462C>T
XM_017011944.1:c.1437G>A XP_016867433.1:p.Met479Ile
XM_017011945.1:c.1437G>A XP_016867434.1:p.Met479Ile
XM_017011946.2:c.1437G>A XP_016867435.1:p.Met479Ile
XM_017011947.1:c.1437G>A XP_016867436.1:p.Met479Ile
XR_928169.2:n.302-16462C>T
XR_928171.2:n.302-16462C>T
NM_001091.4:c.1437G>A VV MANE Preferred NP_001082.2:p.Met479Ile
NM_001272072.2:c.1437G>A VV NP_001259001.1:p.Met479Ile
ENST00000360937.8:c.1437G>A ENSP00000354193.4:p.Met479Ile
ENST00000416793.6:c.1437G>A ENSP00000411613.2:p.Met479Ile
ENST00000467291.5:c.1437G>A ENSP00000418328.1:p.Met479Ile
ENST00000493429.5:c.1437G>A ENSP00000418614.1:p.Met479Ile
ENST00000619575.1:c.1434G>A ENSP00000481717.1:p.Met478Ile
ENST00000622116.4:c.15G>A ENSP00000481520.1:p.Met5Ile