Canonical Allele Identifier: CA1701738254

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999416C= , CM000669.2:g.39999416C=	GRCh38
NC_000007.13:g.40039015C= , CM000669.1:g.40039015C=	GRCh37
NC_000007.12:g.40005540C=	NCBI36
NG_052965.1:g.54057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2098C= MANE Select	ENSP00000181839.4:p.Arg700=
ENST00000340829.10:c.2098C=	ENSP00000340557.5:p.Arg700=
ENST00000484589.2:c.650C=
ENST00000642213.1:n.580C=
ENST00000643859.1:c.989C=
ENST00000643915.1:c.412C=	ENSP00000496187.1:p.Arg138=
ENST00000645470.1:c.28C=	ENSP00000495036.1:p.Arg10=
ENST00000646039.1:c.1438C=	ENSP00000494168.1:p.Arg480=
ENST00000646437.1:c.732C=
ENST00000647453.1:n.1167C=
ENST00000647518.1:n.3935C=
ENST00000181839.8:c.2098C=	ENSP00000181839.4:p.Arg700=
ENST00000340829.9:c.2098C=	ENSP00000340557.5:p.Arg700=
ENST00000484589.1:n.650C=
ENST00000611390.1:c.256C=	ENSP00000484610.1:p.Arg86=
ENST00000613626.4:c.256C=	ENSP00000480835.1:p.Arg86=
NM_003718.4:c.2098C=	NP_003709.3:p.Arg700=
NM_031267.3:c.2098C=	NP_112557.2:p.Arg700=
XM_011515597.1:c.2098C=	XP_011513899.1:p.Arg700=
XM_011515598.1:c.2098C=	XP_011513900.1:p.Arg700=
XM_011515597.3:c.2098C=	XP_011513899.1:p.Arg700=
XM_017012750.2:c.2098C=	XP_016868239.1:p.Arg700=
XM_017012751.2:c.2098C=	XP_016868240.1:p.Arg700=
NM_003718.5:c.2098C= MANE Select	NP_003709.3:p.Arg700=