LDH info

Canonical Allele Identifier: CA6910559
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs760182821

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334059C>T , CM000675.2:g.23334059C>T GRCh38
NC_000013.10:g.23908198C>T , CM000675.1:g.23908198C>T GRCh37
NC_000013.9:g.22806198C>T NCBI36
NG_012342.1:g.104644G>A

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9376G>A VV NP_001264984.1:p.Asp3126Asn
NM_014363.5:c.9817G>A VV NP_055178.3:p.Asp3273Asn
XM_005266338.1:c.9844G>A XP_005266395.1:p.Asp3282Asn
XM_011535038.1:c.9868G>A XP_011533340.1:p.Asp3290Asn
XM_011535039.1:c.9835G>A XP_011533341.1:p.Asp3279Asn
XM_005266338.2:c.9844G>A XP_005266395.1:p.Asp3282Asn
XM_011535039.2:c.9835G>A XP_011533341.1:p.Asp3279Asn
XM_017020539.1:c.9808G>A XP_016876028.1:p.Asp3270Asn
XM_024449337.1:c.9844G>A XP_024305105.1:p.Asp3282Asn
NM_014363.6:c.9817G>A VV MANE Preferred NP_055178.3:p.Asp3273Asn
NM_001278055.2:c.9376G>A VV NP_001264984.1:p.Asp3126Asn
ENST00000382292.7:c.9817G>A ENSP00000371729.3:p.Asp3273Asn
ENST00000382298.7:c.9817G>A ENSP00000371735.3:p.Asp3273Asn
ENST00000402364.1:c.7567G>A ENSP00000385844.1:p.Asp2523Asn
ENST00000423156.1:n.1058-4575G>A ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4575G>A