LDH info

Canonical Allele Identifier: CA13619269
Gene: SLC2A13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1005956

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39947283T>C , CM000674.2:g.39947283T>C GRCh38
NC_000012.11:g.40341085T>C , CM000674.1:g.40341085T>C GRCh37
NC_000012.10:g.38627352T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_052885.3:c.1034+3974A>G VV NP_443117.3:p.=
XM_011537847.1:c.1034+3974A>G XP_011536149.1:p.=
XM_011537848.1:c.1034+3974A>G XP_011536150.1:p.=
XM_011537849.1:c.1034+3974A>G XP_011536151.1:p.=
XM_011537850.1:c.1034+3974A>G XP_011536152.1:p.=
XM_011537847.2:c.1034+3974A>G XP_011536149.1:p.=
XM_011537849.2:c.1034+3974A>G XP_011536151.1:p.=
XM_011537850.3:c.1034+3974A>G XP_011536152.1:p.=
XM_017018764.1:c.467+3974A>G XP_016874253.1:p.=
XM_017018765.1:c.467+3974A>G XP_016874254.1:p.=
XM_017018766.1:c.314+3974A>G XP_016874255.1:p.=
XR_001748567.2:n.1311+3974A>G
XR_001748568.1:n.1311+3974A>G
NM_052885.4:c.1034+3974A>G VV MANE Preferred NP_443117.3:p.=
ENST00000280871.8:c.1034+3974A>G ENSP00000280871.4:p.=