Canonical Allele Identifier: CA454724024
Gene: CDK13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40039068A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999469A>T , CM000669.2:g.39999469A>T GRCh38
NC_000007.13:g.40039068A>T , CM000669.1:g.40039068A>T GRCh37
NC_000007.12:g.40005593A>T NCBI36
NG_052965.1:g.54110A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2151A>T MANE Select ENSP00000181839.4:p.Gly717=
ENST00000340829.10:c.2151A>T ENSP00000340557.5:p.Gly717=
ENST00000484589.2:c.703A>T
ENST00000642213.1:n.633A>T
ENST00000643859.1:c.1042A>T
ENST00000643915.1:c.465A>T ENSP00000496187.1:p.Gly155=
ENST00000645470.1:c.81A>T ENSP00000495036.1:p.Gly27=
ENST00000646039.1:c.1491A>T ENSP00000494168.1:p.Gly497=
ENST00000647453.1:n.1220A>T
ENST00000647518.1:n.3988A>T
ENST00000181839.8:c.2151A>T ENSP00000181839.4:p.Gly717=
ENST00000340829.9:c.2151A>T ENSP00000340557.5:p.Gly717=
ENST00000484589.1:n.703A>T
ENST00000611390.1:c.309A>T ENSP00000484610.1:p.Gly103=
ENST00000613626.4:c.309A>T ENSP00000480835.1:p.Gly103=
NM_003718.4:c.2151A>T NP_003709.3:p.Gly717=
NM_031267.3:c.2151A>T NP_112557.2:p.Gly717=
XM_011515597.1:c.2151A>T XP_011513899.1:p.Gly717=
XM_011515598.1:c.2151A>T XP_011513900.1:p.Gly717=
XM_011515597.3:c.2151A>T XP_011513899.1:p.Gly717=
XM_017012750.2:c.2151A>T XP_016868239.1:p.Gly717=
XM_017012751.2:c.2151A>T XP_016868240.1:p.Gly717=
NM_003718.5:c.2151A>T MANE Select NP_003709.3:p.Gly717=