Canonical Allele Identifier: CA1139655084
Gene: CDK13 HGNC NCBI

Linked Data

dbSNP Id: rs750743833

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40001854T>G , CM000669.2:g.40001854T>G GRCh38
NC_000007.13:g.40041453T>G , CM000669.1:g.40041453T>G GRCh37
NC_000007.12:g.40007978T>G NCBI36
NG_052965.1:g.56495T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2183-7T>G MANE Select ENSP00000181839.4:n.2183-7T>G
ENST00000340829.10:c.2183-7T>G ENSP00000340557.5:n.2183-7T>G
ENST00000484589.2:c.735-7T>G
ENST00000642213.1:n.665-7T>G
ENST00000643859.1:c.1074-7T>G
ENST00000643915.1:c.497-7T>G ENSP00000496187.1:n.497-7T>G
ENST00000645470.1:c.113-7T>G ENSP00000495036.1:n.113-7T>G
ENST00000646039.1:c.1523-7T>G ENSP00000494168.1:n.1523-7T>G
ENST00000647453.1:n.1252-7T>G
ENST00000647518.1:n.4020-7T>G
ENST00000181839.8:c.2183-7T>G ENSP00000181839.4:n.2183-7T>G
ENST00000340829.9:c.2183-7T>G ENSP00000340557.5:n.2183-7T>G
ENST00000484589.1:n.735-7T>G
ENST00000611390.1:c.341-7T>G ENSP00000484610.1:n.341-7T>G
ENST00000613626.4:c.341-7T>G ENSP00000480835.1:n.341-7T>G
NM_003718.4:c.2183-7T>G NP_003709.3:n.2183-7T>G
NM_031267.3:c.2183-7T>G NP_112557.2:n.2183-7T>G
XM_011515597.1:c.2183-7T>G XP_011513899.1:n.2183-7T>G
XM_011515598.1:c.2183-7T>G XP_011513900.1:n.2183-7T>G
XM_011515597.3:c.2183-7T>G XP_011513899.1:n.2183-7T>G
XM_017012750.2:c.2183-7T>G XP_016868239.1:n.2183-7T>G
XM_017012751.2:c.2183-7T>G XP_016868240.1:n.2183-7T>G
NM_003718.5:c.2183-7T>G MANE Select NP_003709.3:n.2183-7T>G