LDH info

Canonical Allele Identifier: CA483159257
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr13:g.23908106A>C (hg19)

Genomic Alleles

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

Transcript Alleles

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