LDH info

Canonical Allele Identifier: CA14915037
Gene: DYRK1A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2835762

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37473496C>T , CM000683.2:g.37473496C>T GRCh38
NC_000021.8:g.38845798C>T , CM000683.1:g.38845798C>T GRCh37
NC_000021.7:g.37767668C>T NCBI36
NG_009366.1:g.110940C>T

Transcript Alleles

HGVS Amino-acid change
NM_001396.3:c.207+616C>T VV NP_001387.2:p.=
NM_101395.2:c.207+616C>T VV NP_567824.1:p.=
NM_130436.2:c.207+616C>T VV NP_569120.1:p.=
NM_130438.2:c.207+616C>T VV NP_569122.1:p.=
XM_005260931.3:c.120+616C>T XP_005260988.1:p.=
XM_006723976.2:c.207+616C>T XP_006724039.1:p.=
XM_006723977.2:c.207+616C>T XP_006724040.1:p.=
XM_006723978.2:c.207+616C>T XP_006724041.1:p.=
XM_006723979.2:c.207+616C>T XP_006724042.1:p.=
XM_011529482.1:c.228+616C>T XP_011527784.1:p.=
XM_011529483.1:c.207+616C>T XP_011527785.1:p.=
XM_011529484.1:c.228+616C>T XP_011527786.1:p.=
XM_011529485.1:c.120+616C>T XP_011527787.1:p.=
NM_001347721.1:c.207+616C>T VV NP_001334650.1:p.=
NM_001347722.1:c.207+616C>T VV NP_001334651.1:p.=
NM_001347723.1:c.120+616C>T VV NP_001334652.1:p.=
NM_001396.4:c.207+616C>T VV NP_001387.2:p.=
XM_006723976.3:c.207+616C>T XP_006724039.1:p.=
XM_006723977.3:c.207+616C>T XP_006724040.1:p.=
XM_006723978.3:c.207+616C>T XP_006724041.1:p.=
XM_011529483.2:c.207+616C>T XP_011527785.1:p.=
XM_017028284.1:c.207+616C>T XP_016883773.1:p.=
XM_017028286.2:c.120+616C>T XP_016883775.1:p.=
XM_024452057.1:c.120+616C>T XP_024307825.1:p.=
NM_001347721.2:c.207+616C>T VV MANE Preferred NP_001334650.1:p.=
NM_001347722.2:c.207+616C>T VV NP_001334651.1:p.=
NM_001347723.2:c.120+616C>T VV NP_001334652.1:p.=
NM_001396.5:c.207+616C>T VV NP_001387.2:p.=
ENST00000338785.7:c.207+616C>T ENSP00000342690.3:p.=
ENST00000339659.8:c.207+616C>T ENSP00000340373.3:p.=
ENST00000398956.2:n.207+616C>T ENSP00000381929.2:p.=
ENST00000398960.6:c.207+616C>T ENSP00000381932.2:p.=
ENST00000426672.5:c.207+616C>T ENSP00000412269.1:p.=
ENST00000462274.1:n.892+616C>T