Canonical Allele Identifier: CA367287989

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40038976T>G (hg19) ; chr7:g.39999377T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999377T>G , CM000669.2:g.39999377T>G	GRCh38
NC_000007.13:g.40038976T>G , CM000669.1:g.40038976T>G	GRCh37
NC_000007.12:g.40005501T>G	NCBI36
NG_052965.1:g.54018T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2059T>G MANE Select	ENSP00000181839.4:p.Tyr687Asp
ENST00000340829.10:c.2059T>G	ENSP00000340557.5:p.Tyr687Asp
ENST00000484589.2:c.611T>G
ENST00000642213.1:n.541T>G
ENST00000642660.1:n.939T>G
ENST00000643859.1:c.950T>G
ENST00000643915.1:c.373T>G	ENSP00000496187.1:p.Tyr125Asp
ENST00000646039.1:c.1399T>G	ENSP00000494168.1:p.Tyr467Asp
ENST00000646437.1:c.693T>G
ENST00000647453.1:n.1128T>G
ENST00000647518.1:n.3896T>G
ENST00000181839.8:c.2059T>G	ENSP00000181839.4:p.Tyr687Asp
ENST00000340829.9:c.2059T>G	ENSP00000340557.5:p.Tyr687Asp
ENST00000484589.1:n.611T>G
ENST00000611390.1:c.217T>G	ENSP00000484610.1:p.Tyr73Asp
ENST00000613626.4:c.217T>G	ENSP00000480835.1:p.Tyr73Asp
NM_003718.4:c.2059T>G	NP_003709.3:p.Tyr687Asp
NM_031267.3:c.2059T>G	NP_112557.2:p.Tyr687Asp
XM_011515597.1:c.2059T>G	XP_011513899.1:p.Tyr687Asp
XM_011515598.1:c.2059T>G	XP_011513900.1:p.Tyr687Asp
XM_011515597.3:c.2059T>G	XP_011513899.1:p.Tyr687Asp
XM_017012750.2:c.2059T>G	XP_016868239.1:p.Tyr687Asp
XM_017012751.2:c.2059T>G	XP_016868240.1:p.Tyr687Asp
NM_003718.5:c.2059T>G MANE Select	NP_003709.3:p.Tyr687Asp