Canonical Allele Identifier: CA573989728

Gene: CDK13

Linked Data

• dbSNP Id: rs1419654198
• gnomAD v2: 7-40039298-TTTTAAAAAGTGTTCC-T
• gnomAD v3: 7-39999699-TTTTAAAAAGTGTTCC-T
• gnomAD v4: 7-39999699-TTTTAAAAAGTGTTCC-T
• MyVariant Identifiers: chr7:g.40039299_40039313del (hg19) ; chr7:g.39999700_39999714del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999704_39999718del , CM000669.2:g.39999704_39999718del	GRCh38
NC_000007.13:g.40039303_40039317del , CM000669.1:g.40039303_40039317del	GRCh37
NC_000007.12:g.40005828_40005842del	NCBI36
NG_052965.1:g.54345_54359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+204_2182+218del MANE Select	ENSP00000181839.4:n.2182+204_2182+218del
ENST00000340829.10:c.2182+204_2182+218del	ENSP00000340557.5:n.2182+204_2182+218del
ENST00000484589.2:c.734+204_734+218del
ENST00000642213.1:n.664+204_664+218del
ENST00000643859.1:c.1073+204_1073+218del
ENST00000643915.1:c.496+204_496+218del	ENSP00000496187.1:n.496+204_496+218del
ENST00000645470.1:c.112+204_112+218del	ENSP00000495036.1:n.112+204_112+218del
ENST00000646039.1:c.1522+204_1522+218del	ENSP00000494168.1:n.1522+204_1522+218del
ENST00000647453.1:n.1251+204_1251+218del
ENST00000647518.1:n.4019+204_4019+218del
ENST00000181839.8:c.2182+204_2182+218del	ENSP00000181839.4:n.2182+204_2182+218del
ENST00000340829.9:c.2182+204_2182+218del	ENSP00000340557.5:n.2182+204_2182+218del
ENST00000484589.1:n.734+204_734+218del
ENST00000611390.1:c.340+204_340+218del	ENSP00000484610.1:n.340+204_340+218del
ENST00000613626.4:c.340+204_340+218del	ENSP00000480835.1:n.340+204_340+218del
NM_003718.4:c.2182+204_2182+218del	NP_003709.3:n.2182+204_2182+218del
NM_031267.3:c.2182+204_2182+218del	NP_112557.2:n.2182+204_2182+218del
XM_011515597.1:c.2182+204_2182+218del	XP_011513899.1:n.2182+204_2182+218del
XM_011515598.1:c.2182+204_2182+218del	XP_011513900.1:n.2182+204_2182+218del
XM_011515597.3:c.2182+204_2182+218del	XP_011513899.1:n.2182+204_2182+218del
XM_017012750.2:c.2182+204_2182+218del	XP_016868239.1:n.2182+204_2182+218del
XM_017012751.2:c.2182+204_2182+218del	XP_016868240.1:n.2182+204_2182+218del
NM_003718.5:c.2182+204_2182+218del MANE Select	NP_003709.3:n.2182+204_2182+218del