LDH info

Canonical Allele Identifier: CA483159512
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr13:g.23908199A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334060A>C , CM000675.2:g.23334060A>C GRCh38
NC_000013.10:g.23908199A>C , CM000675.1:g.23908199A>C GRCh37
NC_000013.9:g.22806199A>C NCBI36
NG_012342.1:g.104643T>G

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9375T>G VV NP_001264984.1:p.Val3125=
NM_014363.5:c.9816T>G VV NP_055178.3:p.Val3272=
XM_005266338.1:c.9843T>G XP_005266395.1:p.Val3281=
XM_011535038.1:c.9867T>G XP_011533340.1:p.Val3289=
XM_011535039.1:c.9834T>G XP_011533341.1:p.Val3278=
XM_005266338.2:c.9843T>G XP_005266395.1:p.Val3281=
XM_011535039.2:c.9834T>G XP_011533341.1:p.Val3278=
XM_017020539.1:c.9807T>G XP_016876028.1:p.Val3269=
XM_024449337.1:c.9843T>G XP_024305105.1:p.Val3281=
NM_014363.6:c.9816T>G VV MANE Preferred NP_055178.3:p.Val3272=
NM_001278055.2:c.9375T>G VV NP_001264984.1:p.Val3125=
ENST00000382292.7:c.9816T>G ENSP00000371729.3:p.Val3272=
ENST00000382298.7:c.9816T>G ENSP00000371735.3:p.Val3272=
ENST00000402364.1:c.7566T>G ENSP00000385844.1:p.Val2522=
ENST00000423156.1:n.1058-4576T>G ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4576T>G