Canonical Allele Identifier: CA4228403

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39951726A>G , CM000669.2:g.39951726A>G	GRCh38
NC_000007.13:g.39991325A>G , CM000669.1:g.39991325A>G	GRCh37
NC_000007.12:g.39957850A>G	NCBI36
NG_052965.1:g.6367A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003718.5:c.1085A>G MANE Select	NP_003709.3:p.Tyr362Cys
ENST00000181839.10:c.1085A>G MANE Select	ENSP00000181839.4:p.Tyr362Cys
NM_003718.4:c.1085A>G	NP_003709.3:p.Tyr362Cys
NM_031267.3:c.1085A>G	NP_112557.2:p.Tyr362Cys
ENST00000181839.8:c.1085A>G	ENSP00000181839.4:p.Tyr362Cys
ENST00000340829.10:c.1085A>G	ENSP00000340557.5:p.Tyr362Cys
ENST00000340829.9:c.1085A>G	ENSP00000340557.5:p.Tyr362Cys
ENST00000611390.1:c.-758A>G	ENSP00000484610.1:n.-758A>G
ENST00000613626.4:c.-758A>G	ENSP00000480835.1:n.-758A>G
ENST00000643868.1:c.709A>G
ENST00000646039.1:c.425A>G	ENSP00000494168.1:p.Tyr142Cys
XM_011515597.1:c.1085A>G	XP_011513899.1:p.Tyr362Cys
XM_011515597.3:c.1085A>G	XP_011513899.1:p.Tyr362Cys
XM_011515598.1:c.1085A>G	XP_011513900.1:p.Tyr362Cys
XM_017012750.2:c.1085A>G	XP_016868239.1:p.Tyr362Cys
XM_017012751.2:c.1085A>G	XP_016868240.1:p.Tyr362Cys