Canonical Allele Identifier: CA365245579

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.110815043A>G , CM000668.2:g.110815043A>G GRCh38
NC_000006.11:g.111136246A>G , CM000668.1:g.111136246A>G GRCh37
NC_000006.10:g.111242939A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368911.8:c.94T>C (CDK19) MANE Select ENSP00000357907.3:p.Tyr32His
ENST00000323817.7:c.-115+528T>C (CDK19) ENSP00000317665.3:n.-115+528T>C
ENST00000368911.7:c.94T>C (CDK19) ENSP00000357907.3:p.Tyr32His
ENST00000413605.6:c.-87T>C (CDK19) ENSP00000410604.3:n.-87T>C
ENST00000457688.5:c.-149T>C (CDK19) ENSP00000415621.1:n.-149T>C
ENST00000460913.1:n.162T>C (CDK19)
ENST00000468997.5:n.83T>C (CDK19)
ENST00000497709.1:n.151+765T>C (CDK19)
ENST00000610605.4:c.-98+228A>G (AMD1) ENSP00000483984.1:n.-98+228A>G
NM_001287215.1:c.-98+228A>G (AMD1) NP_001274144.1:n.-98+228A>G
NM_001300960.1:c.94T>C (CDK19) NP_001287889.1:p.Tyr32His
NM_001300963.1:c.-115+528T>C (CDK19) NP_001287892.1:n.-115+528T>C
NM_001300964.1:c.-53+765T>C (CDK19) NP_001287893.1:n.-53+765T>C
NM_015076.4:c.94T>C (CDK19) NP_055891.1:p.Tyr32His
XM_011535630.1:c.357+765T>C (CDK19) XP_011533932.1:n.357+765T>C
XM_011535631.1:c.357+765T>C (CDK19) XP_011533933.1:n.357+765T>C
XM_011535630.2:c.357+765T>C (CDK19) XP_011533932.1:n.357+765T>C
XM_011535631.2:c.357+765T>C (CDK19) XP_011533933.1:n.357+765T>C
XM_011535632.2:c.357+765T>C (CDK19) XP_011533934.2:n.357+765T>C
XM_017010587.2:c.-368T>C (CDK19) XP_016866076.1:n.-368T>C
XM_017010588.1:c.-292T>C (CDK19) XP_016866077.1:n.-292T>C
XM_024446376.1:c.357+765T>C (CDK19) XP_024302144.1:n.357+765T>C
XM_024446377.1:c.-149T>C (CDK19) XP_024302145.1:n.-149T>C
NM_015076.5:c.94T>C (CDK19) MANE Select NP_055891.1:p.Tyr32His
NM_001300960.2:c.94T>C (CDK19) NP_001287889.1:p.Tyr32His
NM_001300964.2:c.-53+765T>C (CDK19) NP_001287893.1:n.-53+765T>C
NM_001287215.2:c.-98+228A>G (AMD1) NP_001274144.1:n.-98+228A>G
NM_001300963.2:c.-115+528T>C (CDK19) NP_001287892.1:n.-115+528T>C