LDH info

Canonical Allele Identifier: CA387513397
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333969G>A , CM000675.2:g.23333969G>A GRCh38
NC_000013.10:g.23908108G>A , CM000675.1:g.23908108G>A GRCh37
NC_000013.9:g.22806108G>A NCBI36
NG_012342.1:g.104734C>T

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9466C>T VV NP_001264984.1:p.Pro3156Ser
NM_014363.5:c.9907C>T VV NP_055178.3:p.Pro3303Ser
XM_005266338.1:c.9934C>T XP_005266395.1:p.Pro3312Ser
XM_011535038.1:c.9958C>T XP_011533340.1:p.Pro3320Ser
XM_011535039.1:c.9925C>T XP_011533341.1:p.Pro3309Ser
XM_005266338.2:c.9934C>T XP_005266395.1:p.Pro3312Ser
XM_011535039.2:c.9925C>T XP_011533341.1:p.Pro3309Ser
XM_017020539.1:c.9898C>T XP_016876028.1:p.Pro3300Ser
XM_024449337.1:c.9934C>T XP_024305105.1:p.Pro3312Ser
NM_014363.6:c.9907C>T VV MANE Preferred NP_055178.3:p.Pro3303Ser
NM_001278055.2:c.9466C>T VV NP_001264984.1:p.Pro3156Ser
ENST00000382292.7:c.9907C>T ENSP00000371729.3:p.Pro3303Ser
ENST00000382298.7:c.9907C>T ENSP00000371735.3:p.Pro3303Ser
ENST00000402364.1:c.7657C>T ENSP00000385844.1:p.Pro2553Ser
ENST00000423156.1:n.1058-4485C>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4485C>T