LDH info

Canonical Allele Identifier: CA14671788
Gene: CRTC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10038

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18781918C>A , CM000681.2:g.18781918C>A GRCh38
NC_000019.9:g.18892728C>A , CM000681.1:g.18892728C>A GRCh37
NC_000019.8:g.18753728C>A NCBI36
NG_007070.1:g.14387G>T

Transcript Alleles

HGVS Amino-acid change
NM_001098482.1:c.*4536C>A VV NP_001091952.1:p.=
NM_015321.2:c.*4536C>A VV NP_056136.2:p.=
XM_005259833.2:c.*4536C>A XP_005259890.1:p.=
XM_005259834.1:c.*4536C>A XP_005259891.1:p.=
XM_005259835.2:c.*4536C>A XP_005259892.1:p.=
XM_005259836.2:c.*4536C>A XP_005259893.1:p.=
XM_006722710.2:c.*4536C>A XP_006722773.1:p.=
XM_011527842.1:c.*4536C>A XP_011526144.1:p.=
XM_005259833.3:c.*4536C>A XP_005259890.1:p.=
XM_005259835.3:c.*4536C>A XP_005259892.1:p.=
XM_005259836.3:c.*4536C>A XP_005259893.1:p.=
XM_006722710.3:c.*4536C>A XP_006722773.1:p.=
XM_011527842.3:c.*4536C>A XP_011526144.1:p.=
XM_024451434.1:c.*4536C>A XP_024307202.1:p.=
NM_015321.3:c.*4536C>A VV MANE Preferred NP_056136.2:p.=
NM_001098482.2:c.*4536C>A VV NP_001091952.1:p.=
ENST00000338797.10:c.*4536C>A ENSP00000345001.5:p.=