LDH info

Canonical Allele Identifier: CA246652926
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs951426966

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333967A>G , CM000675.2:g.23333967A>G GRCh38
NC_000013.10:g.23908106A>G , CM000675.1:g.23908106A>G GRCh37
NC_000013.9:g.22806106A>G NCBI36
NG_012342.1:g.104736T>C

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9468T>C VV NP_001264984.1:p.Pro3156=
NM_014363.5:c.9909T>C VV NP_055178.3:p.Pro3303=
XM_005266338.1:c.9936T>C XP_005266395.1:p.Pro3312=
XM_011535038.1:c.9960T>C XP_011533340.1:p.Pro3320=
XM_011535039.1:c.9927T>C XP_011533341.1:p.Pro3309=
XM_005266338.2:c.9936T>C XP_005266395.1:p.Pro3312=
XM_011535039.2:c.9927T>C XP_011533341.1:p.Pro3309=
XM_017020539.1:c.9900T>C XP_016876028.1:p.Pro3300=
XM_024449337.1:c.9936T>C XP_024305105.1:p.Pro3312=
NM_014363.6:c.9909T>C VV MANE Preferred NP_055178.3:p.Pro3303=
NM_001278055.2:c.9468T>C VV NP_001264984.1:p.Pro3156=
ENST00000382292.7:c.9909T>C ENSP00000371729.3:p.Pro3303=
ENST00000382298.7:c.9909T>C ENSP00000371735.3:p.Pro3303=
ENST00000402364.1:c.7659T>C ENSP00000385844.1:p.Pro2553=
ENST00000423156.1:n.1058-4483T>C ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4483T>C