Canonical Allele Identifier: CA367289631

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40041536T>G (hg19) ; chr7:g.40001937T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40001937T>G , CM000669.2:g.40001937T>G	GRCh38
NC_000007.13:g.40041536T>G , CM000669.1:g.40041536T>G	GRCh37
NC_000007.12:g.40008061T>G	NCBI36
NG_052965.1:g.56578T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2259T>G MANE Select	ENSP00000181839.4:p.Ile753Met
ENST00000340829.10:c.2259T>G	ENSP00000340557.5:p.Ile753Met
ENST00000484589.2:c.811T>G
ENST00000642213.1:n.741T>G
ENST00000643859.1:c.1150T>G
ENST00000643915.1:c.573T>G	ENSP00000496187.1:p.Ile191Met
ENST00000645470.1:c.189T>G	ENSP00000495036.1:p.Ile63Met
ENST00000646039.1:c.1599T>G	ENSP00000494168.1:p.Ile533Met
ENST00000647453.1:n.1328T>G
ENST00000647518.1:n.4096T>G
ENST00000181839.8:c.2259T>G	ENSP00000181839.4:p.Ile753Met
ENST00000340829.9:c.2259T>G	ENSP00000340557.5:p.Ile753Met
ENST00000484589.1:n.811T>G
ENST00000611390.1:c.417T>G	ENSP00000484610.1:p.Ile139Met
ENST00000613626.4:c.417T>G	ENSP00000480835.1:p.Ile139Met
NM_003718.4:c.2259T>G	NP_003709.3:p.Ile753Met
NM_031267.3:c.2259T>G	NP_112557.2:p.Ile753Met
XM_011515597.1:c.2259T>G	XP_011513899.1:p.Ile753Met
XM_011515598.1:c.2259T>G	XP_011513900.1:p.Ile753Met
XM_011515597.3:c.2259T>G	XP_011513899.1:p.Ile753Met
XM_017012750.2:c.2259T>G	XP_016868239.1:p.Ile753Met
XM_017012751.2:c.2259T>G	XP_016868240.1:p.Ile753Met
NM_003718.5:c.2259T>G MANE Select	NP_003709.3:p.Ile753Met