LDH info

Canonical Allele Identifier: CA6910560
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs766837077

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334061A>C , CM000675.2:g.23334061A>C GRCh38
NC_000013.10:g.23908200A>C , CM000675.1:g.23908200A>C GRCh37
NC_000013.9:g.22806200A>C NCBI36
NG_012342.1:g.104642T>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9374T>G VV NP_001264984.1:p.Val3125Gly
NM_014363.5:c.9815T>G VV NP_055178.3:p.Val3272Gly
XM_005266338.1:c.9842T>G XP_005266395.1:p.Val3281Gly
XM_011535038.1:c.9866T>G XP_011533340.1:p.Val3289Gly
XM_011535039.1:c.9833T>G XP_011533341.1:p.Val3278Gly
XM_005266338.2:c.9842T>G XP_005266395.1:p.Val3281Gly
XM_011535039.2:c.9833T>G XP_011533341.1:p.Val3278Gly
XM_017020539.1:c.9806T>G XP_016876028.1:p.Val3269Gly
XM_024449337.1:c.9842T>G XP_024305105.1:p.Val3281Gly
NM_014363.6:c.9815T>G VV MANE Preferred NP_055178.3:p.Val3272Gly
NM_001278055.2:c.9374T>G VV NP_001264984.1:p.Val3125Gly
ENST00000382292.7:c.9815T>G ENSP00000371729.3:p.Val3272Gly
ENST00000382298.7:c.9815T>G ENSP00000371735.3:p.Val3272Gly
ENST00000402364.1:c.7565T>G ENSP00000385844.1:p.Val2522Gly
ENST00000423156.1:n.1058-4577T>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4577T>G