Canonical Allele Identifier: CA454723480
Gene: CDK13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40085613T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40046014T>C , CM000669.2:g.40046014T>C GRCh38
NC_000007.13:g.40085613T>C , CM000669.1:g.40085613T>C GRCh37
NC_000007.12:g.40052138T>C NCBI36
NG_052965.1:g.100655T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000700485.1:n.268T>C
ENST00000700486.1:n.306T>C
ENST00000700487.1:n.274T>C
ENST00000181839.10:c.2532T>C MANE Select ENSP00000181839.4:p.Leu844=
ENST00000340829.10:c.2532T>C ENSP00000340557.5:p.Leu844=
ENST00000484589.2:c.1084T>C
ENST00000642592.1:c.85T>C
ENST00000643859.1:c.1423T>C
ENST00000643915.1:c.846T>C ENSP00000496187.1:p.Leu282=
ENST00000645470.1:c.462T>C ENSP00000495036.1:p.Leu154=
ENST00000646039.1:c.1872T>C ENSP00000494168.1:p.Leu624=
ENST00000647453.1:n.1601T>C
ENST00000181839.8:c.2532T>C ENSP00000181839.4:p.Leu844=
ENST00000340829.9:c.2532T>C ENSP00000340557.5:p.Leu844=
ENST00000484589.1:n.1084T>C
ENST00000611390.1:c.690T>C ENSP00000484610.1:p.Leu230=
ENST00000613626.4:c.690T>C ENSP00000480835.1:p.Leu230=
NM_003718.4:c.2532T>C NP_003709.3:p.Leu844=
NM_031267.3:c.2532T>C NP_112557.2:p.Leu844=
XM_011515597.1:c.2532T>C XP_011513899.1:p.Leu844=
XM_011515598.1:c.2532T>C XP_011513900.1:p.Leu844=
XM_011515597.3:c.2532T>C XP_011513899.1:p.Leu844=
XM_017012750.2:c.2532T>C XP_016868239.1:p.Leu844=
XM_017012751.2:c.2532T>C XP_016868240.1:p.Leu844=
NM_003718.5:c.2532T>C MANE Select NP_003709.3:p.Leu844=