LDH info

Canonical Allele Identifier: CA254726
Gene: GCH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9285
ClinVar RCV Id: RCV000009868
dbSNP Id: rs104894441

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54865376A>T , CM000676.2:g.54865376A>T GRCh38
NC_000014.8:g.55332094A>T , CM000676.1:g.55332094A>T GRCh37
NC_000014.7:g.54401844A>T NCBI36
NG_008647.1:g.42449T>A

Transcript Alleles

HGVS Amino-acid change
NM_000161.2:c.404T>A VV NP_000152.1:p.Ile135Lys
NM_001024024.1:c.404T>A VV NP_001019195.1:p.Ile135Lys
NM_001024070.1:c.404T>A VV NP_001019241.1:p.Ile135Lys
NM_001024071.1:c.404T>A VV NP_001019242.1:p.Ile135Lys
XM_005267530.1:c.404T>A XP_005267587.1:p.Ile135Lys
XM_011536643.1:c.404T>A XP_011534945.1:p.Ile135Lys
XM_017021218.1:c.110T>A XP_016876707.1:p.Ile37Lys
NM_000161.3:c.404T>A VV MANE Preferred NP_000152.1:p.Ile135Lys
ENST00000254299.8:n.552T>A
ENST00000395514.5:c.404T>A ENSP00000378890.1:p.Ile135Lys
ENST00000395521.6:n.187T>A
ENST00000491895.6:c.404T>A ENSP00000419045.2:p.Ile135Lys
ENST00000536224.2:c.404T>A ENSP00000445246.2:p.Ile135Lys
ENST00000543643.6:c.404T>A ENSP00000444011.2:p.Ile135Lys
ENST00000622544.4:c.404T>A ENSP00000477796.1:p.Ile135Lys