Canonical Allele Identifier: CA367289628

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40041535T>G (hg19) ; chr7:g.40001936T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40001936T>G , CM000669.2:g.40001936T>G	GRCh38
NC_000007.13:g.40041535T>G , CM000669.1:g.40041535T>G	GRCh37
NC_000007.12:g.40008060T>G	NCBI36
NG_052965.1:g.56577T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2258T>G MANE Select	ENSP00000181839.4:p.Ile753Ser
ENST00000340829.10:c.2258T>G	ENSP00000340557.5:p.Ile753Ser
ENST00000484589.2:c.810T>G
ENST00000642213.1:n.740T>G
ENST00000643859.1:c.1149T>G
ENST00000643915.1:c.572T>G	ENSP00000496187.1:p.Ile191Ser
ENST00000645470.1:c.188T>G	ENSP00000495036.1:p.Ile63Ser
ENST00000646039.1:c.1598T>G	ENSP00000494168.1:p.Ile533Ser
ENST00000647453.1:n.1327T>G
ENST00000647518.1:n.4095T>G
ENST00000181839.8:c.2258T>G	ENSP00000181839.4:p.Ile753Ser
ENST00000340829.9:c.2258T>G	ENSP00000340557.5:p.Ile753Ser
ENST00000484589.1:n.810T>G
ENST00000611390.1:c.416T>G	ENSP00000484610.1:p.Ile139Ser
ENST00000613626.4:c.416T>G	ENSP00000480835.1:p.Ile139Ser
NM_003718.4:c.2258T>G	NP_003709.3:p.Ile753Ser
NM_031267.3:c.2258T>G	NP_112557.2:p.Ile753Ser
XM_011515597.1:c.2258T>G	XP_011513899.1:p.Ile753Ser
XM_011515598.1:c.2258T>G	XP_011513900.1:p.Ile753Ser
XM_011515597.3:c.2258T>G	XP_011513899.1:p.Ile753Ser
XM_017012750.2:c.2258T>G	XP_016868239.1:p.Ile753Ser
XM_017012751.2:c.2258T>G	XP_016868240.1:p.Ile753Ser
NM_003718.5:c.2258T>G MANE Select	NP_003709.3:p.Ile753Ser