Canonical Allele Identifier: CA367279856

Gene: CDK13

Linked Data

• gnomAD v4: 7-40045918-T-G
• MyVariant Identifiers: chr7:g.40085517T>G (hg19) ; chr7:g.40045918T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045918T>G , CM000669.2:g.40045918T>G	GRCh38
NC_000007.13:g.40085517T>G , CM000669.1:g.40085517T>G	GRCh37
NC_000007.12:g.40052042T>G	NCBI36
NG_052965.1:g.100559T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700485.1:n.172T>G
ENST00000700486.1:n.210T>G
ENST00000700487.1:n.178T>G
ENST00000181839.10:c.2436T>G MANE Select	ENSP00000181839.4:p.Asn812Lys
ENST00000340829.10:c.2436T>G	ENSP00000340557.5:p.Asn812Lys
ENST00000484589.2:c.988T>G
ENST00000643859.1:c.1327T>G
ENST00000643915.1:c.750T>G	ENSP00000496187.1:p.Asn250Lys
ENST00000645470.1:c.366T>G	ENSP00000495036.1:p.Asn122Lys
ENST00000646039.1:c.1776T>G	ENSP00000494168.1:p.Asn592Lys
ENST00000647453.1:n.1505T>G
ENST00000181839.8:c.2436T>G	ENSP00000181839.4:p.Asn812Lys
ENST00000340829.9:c.2436T>G	ENSP00000340557.5:p.Asn812Lys
ENST00000484589.1:n.988T>G
ENST00000611390.1:c.594T>G	ENSP00000484610.1:p.Asn198Lys
ENST00000613626.4:c.594T>G	ENSP00000480835.1:p.Asn198Lys
NM_003718.4:c.2436T>G	NP_003709.3:p.Asn812Lys
NM_031267.3:c.2436T>G	NP_112557.2:p.Asn812Lys
XM_011515597.1:c.2436T>G	XP_011513899.1:p.Asn812Lys
XM_011515598.1:c.2436T>G	XP_011513900.1:p.Asn812Lys
XM_011515597.3:c.2436T>G	XP_011513899.1:p.Asn812Lys
XM_017012750.2:c.2436T>G	XP_016868239.1:p.Asn812Lys
XM_017012751.2:c.2436T>G	XP_016868240.1:p.Asn812Lys
NM_003718.5:c.2436T>G MANE Select	NP_003709.3:p.Asn812Lys