Canonical Allele Identifier: CA4228476

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39987734G>T , CM000669.2:g.39987734G>T	GRCh38
NC_000007.13:g.40027333G>T , CM000669.1:g.40027333G>T	GRCh37
NC_000007.12:g.39993858G>T	NCBI36
NG_052965.1:g.42375G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003718.5:c.1347G>T MANE Select	NP_003709.3:p.Leu449=
ENST00000181839.10:c.1347G>T MANE Select	ENSP00000181839.4:p.Leu449=
NM_003718.4:c.1347G>T	NP_003709.3:p.Leu449=
NM_031267.3:c.1347G>T	NP_112557.2:p.Leu449=
ENST00000181839.8:c.1347G>T	ENSP00000181839.4:p.Leu449=
ENST00000340829.10:c.1347G>T	ENSP00000340557.5:p.Leu449=
ENST00000340829.9:c.1347G>T	ENSP00000340557.5:p.Leu449=
ENST00000611390.1:c.-496G>T	ENSP00000484610.1:n.-496G>T
ENST00000613626.4:c.-496G>T	ENSP00000480835.1:n.-496G>T
ENST00000642626.1:c.136G>T
ENST00000642660.1:n.136G>T
ENST00000643859.1:c.238G>T
ENST00000646039.1:c.687G>T	ENSP00000494168.1:p.Leu229=
ENST00000647518.1:n.3184G>T
XM_011515597.1:c.1347G>T	XP_011513899.1:p.Leu449=
XM_011515597.3:c.1347G>T	XP_011513899.1:p.Leu449=
XM_011515598.1:c.1347G>T	XP_011513900.1:p.Leu449=
XM_017012750.2:c.1347G>T	XP_016868239.1:p.Leu449=
XM_017012751.2:c.1347G>T	XP_016868240.1:p.Leu449=