LDH info

Canonical Allele Identifier: CA354362521
Gene: CASR HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122257160C>A , CM000665.2:g.122257160C>A GRCh38
NC_000003.11:g.121976007C>A , CM000665.1:g.121976007C>A GRCh37
NC_000003.10:g.123458697C>A NCBI36
NG_009058.1:g.78478C>A
NG_009058.2:g.78493C>A

Transcript Alleles

HGVS Amino-acid change
NM_000388.3:c.265C>A VV NP_000379.2:p.Pro89Thr
NM_001178065.1:c.265C>A VV NP_001171536.1:p.Pro89Thr
XM_005247836.2:c.265C>A XP_005247893.1:p.Pro89Thr
XM_005247837.2:c.9+2786C>A XP_005247894.1:p.=
XM_006713789.2:c.265C>A XP_006713852.1:p.Pro89Thr
XM_011513237.1:c.265C>A XP_011511539.1:p.Pro89Thr
XM_011513238.1:c.265C>A XP_011511540.1:p.Pro89Thr
XM_006713789.3:c.265C>A XP_006713852.1:p.Pro89Thr
XM_017007324.1:c.265C>A XP_016862813.1:p.Pro89Thr
XM_017007325.1:c.265C>A XP_016862814.1:p.Pro89Thr
NM_000388.4:c.265C>A VV MANE Preferred NP_000379.3:p.Pro89Thr
NM_001178065.2:c.265C>A VV NP_001171536.2:p.Pro89Thr
ENST00000490131.5:c.265C>A ENSP00000418685.1:p.Pro89Thr
ENST00000490186.1:n.124C>A
ENST00000498619.2:c.265C>A ENSP00000420194.1:p.Pro89Thr