LDH info

Canonical Allele Identifier: CA387513391
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9469C>T VV NP_001264984.1:p.Leu3157Phe
NM_014363.5:c.9910C>T VV NP_055178.3:p.Leu3304Phe
XM_005266338.1:c.9937C>T XP_005266395.1:p.Leu3313Phe
XM_011535038.1:c.9961C>T XP_011533340.1:p.Leu3321Phe
XM_011535039.1:c.9928C>T XP_011533341.1:p.Leu3310Phe
XM_005266338.2:c.9937C>T XP_005266395.1:p.Leu3313Phe
XM_011535039.2:c.9928C>T XP_011533341.1:p.Leu3310Phe
XM_017020539.1:c.9901C>T XP_016876028.1:p.Leu3301Phe
XM_024449337.1:c.9937C>T XP_024305105.1:p.Leu3313Phe
NM_014363.6:c.9910C>T VV MANE Preferred NP_055178.3:p.Leu3304Phe
NM_001278055.2:c.9469C>T VV NP_001264984.1:p.Leu3157Phe
ENST00000382292.7:c.9910C>T ENSP00000371729.3:p.Leu3304Phe
ENST00000382298.7:c.9910C>T ENSP00000371735.3:p.Leu3304Phe
ENST00000402364.1:c.7660C>T ENSP00000385844.1:p.Leu2554Phe
ENST00000423156.1:n.1058-4482C>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4482C>T