Canonical Allele Identifier: CA367290284

Gene: CDK13

Linked Data

• gnomAD v4: 7-40002031-G-T
• MyVariant Identifiers: chr7:g.40041630G>T (hg19) ; chr7:g.40002031G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40002031G>T , CM000669.2:g.40002031G>T	GRCh38
NC_000007.13:g.40041630G>T , CM000669.1:g.40041630G>T	GRCh37
NC_000007.12:g.40008155G>T	NCBI36
NG_052965.1:g.56672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2353G>T MANE Select	ENSP00000181839.4:p.Gly785Cys
ENST00000340829.10:c.2353G>T	ENSP00000340557.5:p.Gly785Cys
ENST00000484589.2:c.905G>T
ENST00000642213.1:n.835G>T
ENST00000643859.1:c.1244G>T
ENST00000643915.1:c.667G>T	ENSP00000496187.1:p.Gly223Cys
ENST00000645470.1:c.283G>T	ENSP00000495036.1:p.Gly95Cys
ENST00000646039.1:c.1693G>T	ENSP00000494168.1:p.Gly565Cys
ENST00000647453.1:n.1422G>T
ENST00000647518.1:n.4190G>T
ENST00000181839.8:c.2353G>T	ENSP00000181839.4:p.Gly785Cys
ENST00000340829.9:c.2353G>T	ENSP00000340557.5:p.Gly785Cys
ENST00000484589.1:n.905G>T
ENST00000611390.1:c.511G>T	ENSP00000484610.1:p.Gly171Cys
ENST00000613626.4:c.511G>T	ENSP00000480835.1:p.Gly171Cys
NM_003718.4:c.2353G>T	NP_003709.3:p.Gly785Cys
NM_031267.3:c.2353G>T	NP_112557.2:p.Gly785Cys
XM_011515597.1:c.2353G>T	XP_011513899.1:p.Gly785Cys
XM_011515598.1:c.2353G>T	XP_011513900.1:p.Gly785Cys
XM_011515597.3:c.2353G>T	XP_011513899.1:p.Gly785Cys
XM_017012750.2:c.2353G>T	XP_016868239.1:p.Gly785Cys
XM_017012751.2:c.2353G>T	XP_016868240.1:p.Gly785Cys
NM_003718.5:c.2353G>T MANE Select	NP_003709.3:p.Gly785Cys