Canonical Allele Identifier: CA454723996

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039023G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999424G>T , CM000669.2:g.39999424G>T	GRCh38
NC_000007.13:g.40039023G>T , CM000669.1:g.40039023G>T	GRCh37
NC_000007.12:g.40005548G>T	NCBI36
NG_052965.1:g.54065G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2106G>T MANE Select	ENSP00000181839.4:p.Val702=
ENST00000340829.10:c.2106G>T	ENSP00000340557.5:p.Val702=
ENST00000484589.2:c.658G>T
ENST00000642213.1:n.588G>T
ENST00000643859.1:c.997G>T
ENST00000643915.1:c.420G>T	ENSP00000496187.1:p.Val140=
ENST00000645470.1:c.36G>T	ENSP00000495036.1:p.Val12=
ENST00000646039.1:c.1446G>T	ENSP00000494168.1:p.Val482=
ENST00000646437.1:c.740G>T
ENST00000647453.1:n.1175G>T
ENST00000647518.1:n.3943G>T
ENST00000181839.8:c.2106G>T	ENSP00000181839.4:p.Val702=
ENST00000340829.9:c.2106G>T	ENSP00000340557.5:p.Val702=
ENST00000484589.1:n.658G>T
ENST00000611390.1:c.264G>T	ENSP00000484610.1:p.Val88=
ENST00000613626.4:c.264G>T	ENSP00000480835.1:p.Val88=
NM_003718.4:c.2106G>T	NP_003709.3:p.Val702=
NM_031267.3:c.2106G>T	NP_112557.2:p.Val702=
XM_011515597.1:c.2106G>T	XP_011513899.1:p.Val702=
XM_011515598.1:c.2106G>T	XP_011513900.1:p.Val702=
XM_011515597.3:c.2106G>T	XP_011513899.1:p.Val702=
XM_017012750.2:c.2106G>T	XP_016868239.1:p.Val702=
XM_017012751.2:c.2106G>T	XP_016868240.1:p.Val702=
NM_003718.5:c.2106G>T MANE Select	NP_003709.3:p.Val702=