LDH info

Canonical Allele Identifier: CA6910556
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs761346441

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334051T>C , CM000675.2:g.23334051T>C GRCh38
NC_000013.10:g.23908190T>C , CM000675.1:g.23908190T>C GRCh37
NC_000013.9:g.22806190T>C NCBI36
NG_012342.1:g.104652A>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9384A>G VV NP_001264984.1:p.Leu3128=
NM_014363.5:c.9825A>G VV NP_055178.3:p.Leu3275=
XM_005266338.1:c.9852A>G XP_005266395.1:p.Leu3284=
XM_011535038.1:c.9876A>G XP_011533340.1:p.Leu3292=
XM_011535039.1:c.9843A>G XP_011533341.1:p.Leu3281=
XM_005266338.2:c.9852A>G XP_005266395.1:p.Leu3284=
XM_011535039.2:c.9843A>G XP_011533341.1:p.Leu3281=
XM_017020539.1:c.9816A>G XP_016876028.1:p.Leu3272=
XM_024449337.1:c.9852A>G XP_024305105.1:p.Leu3284=
NM_014363.6:c.9825A>G VV MANE Preferred NP_055178.3:p.Leu3275=
NM_001278055.2:c.9384A>G VV NP_001264984.1:p.Leu3128=
ENST00000382292.7:c.9825A>G ENSP00000371729.3:p.Leu3275=
ENST00000382298.7:c.9825A>G ENSP00000371735.3:p.Leu3275=
ENST00000402364.1:c.7575A>G ENSP00000385844.1:p.Leu2525=
ENST00000423156.1:n.1058-4567A>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4567A>G