LDH info

Canonical Allele Identifier: CA387513392
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333966G>C , CM000675.2:g.23333966G>C GRCh38
NC_000013.10:g.23908105G>C , CM000675.1:g.23908105G>C GRCh37
NC_000013.9:g.22806105G>C NCBI36
NG_012342.1:g.104737C>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9469C>G VV NP_001264984.1:p.Leu3157Val
NM_014363.5:c.9910C>G VV NP_055178.3:p.Leu3304Val
XM_005266338.1:c.9937C>G XP_005266395.1:p.Leu3313Val
XM_011535038.1:c.9961C>G XP_011533340.1:p.Leu3321Val
XM_011535039.1:c.9928C>G XP_011533341.1:p.Leu3310Val
XM_005266338.2:c.9937C>G XP_005266395.1:p.Leu3313Val
XM_011535039.2:c.9928C>G XP_011533341.1:p.Leu3310Val
XM_017020539.1:c.9901C>G XP_016876028.1:p.Leu3301Val
XM_024449337.1:c.9937C>G XP_024305105.1:p.Leu3313Val
NM_014363.6:c.9910C>G VV MANE Preferred NP_055178.3:p.Leu3304Val
NM_001278055.2:c.9469C>G VV NP_001264984.1:p.Leu3157Val
ENST00000382292.7:c.9910C>G ENSP00000371729.3:p.Leu3304Val
ENST00000382298.7:c.9910C>G ENSP00000371735.3:p.Leu3304Val
ENST00000402364.1:c.7660C>G ENSP00000385844.1:p.Leu2554Val
ENST00000423156.1:n.1058-4482C>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4482C>G