LDH info

Canonical Allele Identifier: CA255264
Gene: COL4A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10462
ClinVar RCV Id: RCV000011208
dbSNP Id: rs104886121

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108597042G>T , CM000685.2:g.108597042G>T GRCh38
NC_000023.10:g.107840272G>T , CM000685.1:g.107840272G>T GRCh37
NC_000023.9:g.107726928G>T NCBI36
NG_011977.1:g.162119G>T
NG_011977.2:g.162119G>T

Transcript Alleles

HGVS Amino-acid change
NM_000495.4:c.1561G>T VV NP_000486.1:p.Gly521Cys
NM_033380.2:c.1561G>T VV NP_203699.1:p.Gly521Cys
XM_005262070.2:c.1561G>T XP_005262127.1:p.Gly521Cys
XM_005262072.3:c.1561G>T XP_005262129.1:p.Gly521Cys
XM_006724616.2:c.1561G>T XP_006724679.1:p.Gly521Cys
XM_011530849.1:c.1237G>T XP_011529151.1:p.Gly413Cys
XM_011530850.1:c.1561G>T XP_011529152.1:p.Gly521Cys
XM_011530849.2:c.1576G>T XP_011529151.2:p.Gly526Cys
XM_017029259.2:c.1576G>T XP_016884748.1:p.Gly526Cys
XM_017029260.1:c.1576G>T XP_016884749.1:p.Gly526Cys
XM_017029261.1:c.1576G>T XP_016884750.1:p.Gly526Cys
XM_017029262.2:c.1576G>T XP_016884751.1:p.Gly526Cys
XM_017029263.2:c.-105G>T XP_016884752.1:p.=
NM_000495.5:c.1561G>T VV NP_000486.1:p.Gly521Cys
NM_033380.3:c.1561G>T VV MANE Preferred NP_203699.1:p.Gly521Cys
ENST00000328300.10:c.1561G>T ENSP00000331902.6:p.Gly521Cys
ENST00000361603.6:c.1561G>T ENSP00000354505.2:p.Gly521Cys
ENST00000483338.1:n.1017G>T