Canonical Allele Identifier: CA2714192793
Gene: CDK13 HGNC NCBI

Linked Data

dbSNP Id: rs1759053828

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999278G>C , CM000669.2:g.39999278G>C GRCh38
NC_000007.13:g.40038877G>C , CM000669.1:g.40038877G>C GRCh37
NC_000007.12:g.40005402G>C NCBI36
NG_052965.1:g.53919G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2043-83G>C MANE Select ENSP00000181839.4:n.2043-83G>C
ENST00000340829.10:c.2043-83G>C ENSP00000340557.5:n.2043-83G>C
ENST00000484589.2:c.595-83G>C
ENST00000642213.1:n.442G>C
ENST00000642660.1:n.923-83G>C
ENST00000643859.1:c.934-83G>C
ENST00000643915.1:c.357-83G>C ENSP00000496187.1:n.357-83G>C
ENST00000646039.1:c.1383-83G>C ENSP00000494168.1:n.1383-83G>C
ENST00000646437.1:c.662-68G>C
ENST00000647453.1:n.1029G>C
ENST00000647518.1:n.3880-83G>C
ENST00000181839.8:c.2043-83G>C ENSP00000181839.4:n.2043-83G>C
ENST00000340829.9:c.2043-83G>C ENSP00000340557.5:n.2043-83G>C
ENST00000484589.1:n.595-83G>C
ENST00000611390.1:c.201-83G>C ENSP00000484610.1:n.201-83G>C
ENST00000613626.4:c.201-83G>C ENSP00000480835.1:n.201-83G>C
NM_003718.4:c.2043-83G>C NP_003709.3:n.2043-83G>C
NM_031267.3:c.2043-83G>C NP_112557.2:n.2043-83G>C
XM_011515597.1:c.2043-83G>C XP_011513899.1:n.2043-83G>C
XM_011515598.1:c.2043-83G>C XP_011513900.1:n.2043-83G>C
XM_011515597.3:c.2043-83G>C XP_011513899.1:n.2043-83G>C
XM_017012750.2:c.2043-83G>C XP_016868239.1:n.2043-83G>C
XM_017012751.2:c.2043-83G>C XP_016868240.1:n.2043-83G>C
NM_003718.5:c.2043-83G>C MANE Select NP_003709.3:n.2043-83G>C