Canonical Allele Identifier: CA573989671

Gene: CDK13

Linked Data

• dbSNP Id: rs1244222961
• gnomAD v2: 7-40038883-G-GAGTAGATATTGAGTTATTAGAC
• gnomAD v3: 7-39999284-G-GAGTAGATATTGAGTTATTAGAC
• gnomAD v4: 7-39999284-G-GAGTAGATATTGAGTTATTAGAC
• MyVariant Identifiers: chr7:g.40038883_40038884insAGTAGATATTGAGTTATTAGAC (hg19) ; chr7:g.39999284_39999285insAGTAGATATTGAGTTATTAGAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999288_39999309dup , CM000669.2:g.39999288_39999309dup	GRCh38
NC_000007.13:g.40038887_40038908dup , CM000669.1:g.40038887_40038908dup	GRCh37
NC_000007.12:g.40005412_40005433dup	NCBI36
NG_052965.1:g.53929_53950dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2043-73_2043-52dup MANE Select	ENSP00000181839.4:n.2043-73_2043-52dup
ENST00000340829.10:c.2043-73_2043-52dup	ENSP00000340557.5:n.2043-73_2043-52dup
ENST00000484589.2:c.595-73_595-52dup
ENST00000642213.1:n.452_473dup
ENST00000642660.1:n.923-73_923-52dup
ENST00000643859.1:c.934-73_934-52dup
ENST00000643915.1:c.357-73_357-52dup	ENSP00000496187.1:n.357-73_357-52dup
ENST00000646039.1:c.1383-73_1383-52dup	ENSP00000494168.1:n.1383-73_1383-52dup
ENST00000646437.1:c.662-58_662-37dup
ENST00000647453.1:n.1039_1060dup
ENST00000647518.1:n.3880-73_3880-52dup
ENST00000181839.8:c.2043-73_2043-52dup	ENSP00000181839.4:n.2043-73_2043-52dup
ENST00000340829.9:c.2043-73_2043-52dup	ENSP00000340557.5:n.2043-73_2043-52dup
ENST00000484589.1:n.595-73_595-52dup
ENST00000611390.1:c.201-73_201-52dup	ENSP00000484610.1:n.201-73_201-52dup
ENST00000613626.4:c.201-73_201-52dup	ENSP00000480835.1:n.201-73_201-52dup
NM_003718.4:c.2043-73_2043-52dup	NP_003709.3:n.2043-73_2043-52dup
NM_031267.3:c.2043-73_2043-52dup	NP_112557.2:n.2043-73_2043-52dup
XM_011515597.1:c.2043-73_2043-52dup	XP_011513899.1:n.2043-73_2043-52dup
XM_011515598.1:c.2043-73_2043-52dup	XP_011513900.1:n.2043-73_2043-52dup
XM_011515597.3:c.2043-73_2043-52dup	XP_011513899.1:n.2043-73_2043-52dup
XM_017012750.2:c.2043-73_2043-52dup	XP_016868239.1:n.2043-73_2043-52dup
XM_017012751.2:c.2043-73_2043-52dup	XP_016868240.1:n.2043-73_2043-52dup
NM_003718.5:c.2043-73_2043-52dup MANE Select	NP_003709.3:n.2043-73_2043-52dup