Canonical Allele Identifier: CA367288358

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039061C>G (hg19) ; chr7:g.39999462C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999462C>G , CM000669.2:g.39999462C>G	GRCh38
NC_000007.13:g.40039061C>G , CM000669.1:g.40039061C>G	GRCh37
NC_000007.12:g.40005586C>G	NCBI36
NG_052965.1:g.54103C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2144C>G MANE Select	ENSP00000181839.4:p.Thr715Ser
ENST00000340829.10:c.2144C>G	ENSP00000340557.5:p.Thr715Ser
ENST00000484589.2:c.696C>G
ENST00000642213.1:n.626C>G
ENST00000643859.1:c.1035C>G
ENST00000643915.1:c.458C>G	ENSP00000496187.1:p.Thr153Ser
ENST00000645470.1:c.74C>G	ENSP00000495036.1:p.Thr25Ser
ENST00000646039.1:c.1484C>G	ENSP00000494168.1:p.Thr495Ser
ENST00000647453.1:n.1213C>G
ENST00000647518.1:n.3981C>G
ENST00000181839.8:c.2144C>G	ENSP00000181839.4:p.Thr715Ser
ENST00000340829.9:c.2144C>G	ENSP00000340557.5:p.Thr715Ser
ENST00000484589.1:n.696C>G
ENST00000611390.1:c.302C>G	ENSP00000484610.1:p.Thr101Ser
ENST00000613626.4:c.302C>G	ENSP00000480835.1:p.Thr101Ser
NM_003718.4:c.2144C>G	NP_003709.3:p.Thr715Ser
NM_031267.3:c.2144C>G	NP_112557.2:p.Thr715Ser
XM_011515597.1:c.2144C>G	XP_011513899.1:p.Thr715Ser
XM_011515598.1:c.2144C>G	XP_011513900.1:p.Thr715Ser
XM_011515597.3:c.2144C>G	XP_011513899.1:p.Thr715Ser
XM_017012750.2:c.2144C>G	XP_016868239.1:p.Thr715Ser
XM_017012751.2:c.2144C>G	XP_016868240.1:p.Thr715Ser
NM_003718.5:c.2144C>G MANE Select	NP_003709.3:p.Thr715Ser