Canonical Allele Identifier: CA367285887

Gene: CDK13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40062911G>A , CM000669.2:g.40062911G>A	GRCh38
NC_000007.13:g.40102510G>A , CM000669.1:g.40102510G>A	GRCh37
NC_000007.12:g.40069035G>A	NCBI36
NG_052965.1:g.117552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700485.1:n.422G>A
ENST00000700486.1:n.460G>A
ENST00000700487.1:n.428G>A
ENST00000181839.10:c.2686G>A MANE Select	ENSP00000181839.4:p.Asp896Asn
ENST00000340829.10:c.2686G>A	ENSP00000340557.5:p.Asp896Asn
ENST00000478563.2:n.151G>A
ENST00000484589.2:c.1238G>A
ENST00000642592.1:c.239G>A
ENST00000643859.1:c.1577G>A
ENST00000643915.1:c.1000G>A	ENSP00000496187.1:p.Asp334Asn
ENST00000644221.1:n.2092G>A
ENST00000644561.1:n.401G>A
ENST00000645470.1:c.616G>A	ENSP00000495036.1:p.Asp206Asn
ENST00000646039.1:c.2026G>A	ENSP00000494168.1:p.Asp676Asn
ENST00000181839.8:c.2686G>A	ENSP00000181839.4:p.Asp896Asn
ENST00000340829.9:c.2686G>A	ENSP00000340557.5:p.Asp896Asn
ENST00000484589.1:n.1238G>A
ENST00000611390.1:c.844G>A	ENSP00000484610.1:p.Asp282Asn
ENST00000613626.4:c.844G>A	ENSP00000480835.1:p.Asp282Asn
NM_003718.4:c.2686G>A	NP_003709.3:p.Asp896Asn
NM_031267.3:c.2686G>A	NP_112557.2:p.Asp896Asn
XM_017012750.2:c.2776G>A	XP_016868239.1:p.Asp926Asn
XM_017012751.2:c.2776G>A	XP_016868240.1:p.Asp926Asn
NM_003718.5:c.2686G>A MANE Select	NP_003709.3:p.Asp896Asn