LDH info

Canonical Allele Identifier: CA13000816
Gene: FPGS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10106

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127813796T>C , CM000671.2:g.127813796T>C GRCh38
NC_000009.11:g.130576075T>C , CM000671.1:g.130576075T>C GRCh37
NC_000009.10:g.129615896T>C NCBI36
NG_009551.1:g.45973A>G , LRG_589:g.45973A>G
NG_023245.1:g.15922T>C

Transcript Alleles

HGVS Amino-acid change
NM_001018078.2:c.*192T>C VV NP_001018088.1:p.=
NM_001288803.1:c.*192T>C VV NP_001275732.1:p.=
NM_004957.5:c.*192T>C VV NP_004948.4:p.=
NR_110170.1:n.2004T>C
XM_005251864.2:c.1484-412T>C XP_005251921.1:p.=
XM_011518437.1:c.*192T>C XP_011516739.1:p.=
XM_011518438.1:c.*192T>C XP_011516740.1:p.=
XM_011518439.1:c.*192T>C XP_011516741.1:p.=
XR_242581.2:n.1853T>C
XR_242582.2:n.1381-412T>C
XM_005251864.4:c.1484-412T>C XP_005251921.1:p.=
XM_011518439.2:c.*192T>C XP_011516741.1:p.=
XM_017014565.2:c.1334-412T>C XP_016870054.1:p.=
XM_017014566.1:c.*192T>C XP_016870055.1:p.=
XR_242581.4:n.1851T>C
XR_242582.4:n.1379-412T>C
ENST00000373225.7:c.*192T>C ENSP00000362322.3:p.=
ENST00000373247.6:c.*192T>C ENSP00000362344.2:p.=
ENST00000393706.6:c.*192T>C ENSP00000377309.2:p.=
ENST00000460181.5:n.1944T>C
ENST00000467826.5:n.710-412T>C
ENST00000630236.2:c.*680T>C ENSP00000486766.1:p.=