Canonical Allele Identifier: CA2466399733

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592554G= , CM000685.2:g.153592554G=	GRCh38
NC_000023.10:g.152858012G= , CM000685.1:g.152858012G=	GRCh37
NC_000023.9:g.152511206G=	NCBI36
NG_008393.2:g.11624C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000576892.8:c.609C= MANE Select	ENSP00000461135.1:p.Tyr203=
ENST00000429336.5:c.193+1993C=
ENST00000440428.5:c.609C=	ENSP00000402949.2:p.Tyr203=
ENST00000576892.7:c.609C=	ENSP00000461135.1:p.Tyr203=
ENST00000614850.1:c.277+3450C=
ENST00000614851.4:c.430C=
ENST00000620088.4:c.*485C=	ENSP00000484108.1:n.*485C=
ENST00000621629.4:c.*485C=	ENSP00000478747.1:n.*485C=
NM_001130997.2:c.609C=	NP_001124469.1:p.Tyr203=
NM_152274.4:c.609C=	NP_689487.2:p.Tyr203=
XM_005277920.3:c.579C=	XP_005277977.1:p.Tyr193=
XM_005277921.3:c.579C=	XP_005277978.1:p.Tyr193=
XM_011531213.1:c.483C=	XP_011529515.1:p.Tyr161=
XM_011531214.1:c.483C=	XP_011529516.1:p.Tyr161=
XM_011531215.1:c.483C=	XP_011529517.1:p.Tyr161=
XM_005277920.4:c.579C=	XP_005277977.1:p.Tyr193=
XM_005277921.4:c.579C=	XP_005277978.1:p.Tyr193=
XM_011531214.2:c.483C=	XP_011529516.1:p.Tyr161=
XM_011531215.2:c.483C=	XP_011529517.1:p.Tyr161=
XR_002958810.1:n.2514C=
NM_152274.5:c.609C= MANE Select	NP_689487.2:p.Tyr203=
NM_001130997.3:c.609C=	NP_001124469.1:p.Tyr203=