LDH info

Canonical Allele Identifier: CA483159237
Gene: SACS HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr13:g.23908097A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333958A>G , CM000675.2:g.23333958A>G GRCh38
NC_000013.10:g.23908097A>G , CM000675.1:g.23908097A>G GRCh37
NC_000013.9:g.22806097A>G NCBI36
NG_012342.1:g.104745T>C

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9477T>C VV NP_001264984.1:p.Leu3159=
NM_014363.5:c.9918T>C VV NP_055178.3:p.Leu3306=
XM_005266338.1:c.9945T>C XP_005266395.1:p.Leu3315=
XM_011535038.1:c.9969T>C XP_011533340.1:p.Leu3323=
XM_011535039.1:c.9936T>C XP_011533341.1:p.Leu3312=
XM_005266338.2:c.9945T>C XP_005266395.1:p.Leu3315=
XM_011535039.2:c.9936T>C XP_011533341.1:p.Leu3312=
XM_017020539.1:c.9909T>C XP_016876028.1:p.Leu3303=
XM_024449337.1:c.9945T>C XP_024305105.1:p.Leu3315=
NM_014363.6:c.9918T>C VV MANE Preferred NP_055178.3:p.Leu3306=
NM_001278055.2:c.9477T>C VV NP_001264984.1:p.Leu3159=
ENST00000382292.7:c.9918T>C ENSP00000371729.3:p.Leu3306=
ENST00000382298.7:c.9918T>C ENSP00000371735.3:p.Leu3306=
ENST00000402364.1:c.7668T>C ENSP00000385844.1:p.Leu2556=
ENST00000423156.1:n.1058-4474T>C ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4474T>C