Canonical Allele Identifier: CA1139829471

Gene: PAQR6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156243466G= , CM000663.2:g.156243466G=	GRCh38
NC_000001.10:g.156213257G= , CM000663.1:g.156213257G=	GRCh37
NC_000001.9:g.154479881G=	NCBI36
NG_047015.1:g.6307G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292291.10:c.*663C= MANE Select	ENSP00000292291.5:n.*663C=
ENST00000335852.6:c.*395C=	ENSP00000338330.1:n.*395C=
ENST00000340183.10:c.*1040C=	ENSP00000341926.6:n.*1040C=
ENST00000491107.6:n.1755C=
ENST00000649372.1:n.2067C=
ENST00000292291.9:c.*663C=	ENSP00000292291.5:n.*663C=
ENST00000335852.5:c.*395C=	ENSP00000338330.1:n.*395C=
ENST00000340183.9:c.1755C=	ENSP00000341926.5:n.1755C=
ENST00000356983.6:c.*663C=	ENSP00000349474.3:n.*663C=
ENST00000368270.2:c.*663C=	ENSP00000357253.1:n.*663C=
ENST00000468632.5:n.1980C=
ENST00000491107.5:n.1738C=
ENST00000492619.5:n.1978C=
ENST00000540423.5:c.*395C=	ENSP00000443167.2:n.*395C=
ENST00000612424.4:c.*395C=	ENSP00000482685.1:n.*395C=
ENST00000613336.4:c.*395C=	ENSP00000479864.1:n.*395C=
ENST00000623241.3:c.*395C=	ENSP00000485607.1:n.*395C=
NM_001272104.1:c.*663C=	NP_001259033.1:n.*663C=
NM_001272105.1:c.*663C=	NP_001259034.1:n.*663C=
NM_001272106.1:c.*395C=	NP_001259035.1:n.*395C=
NM_001272107.1:c.*663C=	NP_001259036.1:n.*663C=
NM_001272108.1:c.*663C=	NP_001259037.1:n.*663C=
NM_001272109.1:c.*395C=	NP_001259038.1:n.*395C=
NM_001272110.1:c.*395C=	NP_001259039.1:n.*395C=
NM_001272111.1:c.*395C=	NP_001259040.1:n.*395C=
NM_001272112.1:c.*395C=	NP_001259041.1:n.*395C=
NM_001272113.1:c.*395C=	NP_001259042.1:n.*395C=
NM_024897.3:c.*395C=	NP_079173.2:n.*395C=
NM_198406.2:c.*663C=	NP_940798.1:n.*663C=
NR_073610.1:n.1808C=
XM_005245494.2:c.*395C=	XP_005245551.1:n.*395C=
XM_006711546.1:c.*395C=	XP_006711609.1:n.*395C=
XM_006711547.2:c.*395C=	XP_006711610.1:n.*395C=
XM_006711548.2:c.*395C=	XP_006711611.1:n.*395C=
XM_006711549.2:c.*395C=	XP_006711612.1:n.*395C=
XM_006711552.1:c.*395C=	XP_006711615.1:n.*395C=
XM_006711553.2:c.*395C=	XP_006711616.1:n.*395C=
XM_006711554.2:c.*663C=	XP_006711617.1:n.*663C=
XM_011509999.1:c.*395C=	XP_011508301.1:n.*395C=
XM_011510000.1:c.*395C=	XP_011508302.1:n.*395C=
XR_426796.2:n.2160C=
XR_921951.1:n.1727C=
XM_005245494.4:c.*395C=	XP_005245551.1:n.*395C=
XM_006711546.2:c.*395C=	XP_006711609.1:n.*395C=
XM_006711547.4:c.*395C=	XP_006711610.1:n.*395C=
XM_006711548.4:c.*395C=	XP_006711611.1:n.*395C=
XM_006711552.3:c.*395C=	XP_006711615.1:n.*395C=
XM_006711553.4:c.*395C=	XP_006711616.1:n.*395C=
XM_024449878.1:c.*395C=	XP_024305646.1:n.*395C=
XM_024449879.1:c.*395C=	XP_024305647.1:n.*395C=
XM_024449880.1:c.*395C=	XP_024305648.1:n.*395C=
XM_024449881.1:c.*395C=	XP_024305649.1:n.*395C=
XR_001737427.1:n.1798C=
XR_001737428.2:n.1767C=
XR_002957631.1:n.1727C=
NM_001272104.2:c.*663C=	NP_001259033.1:n.*663C=
NM_001272105.2:c.*663C=	NP_001259034.1:n.*663C=
NM_001272107.2:c.*663C=	NP_001259036.1:n.*663C=
NM_001272108.2:c.*663C=	NP_001259037.1:n.*663C=
NM_001272110.2:c.*395C=	NP_001259039.1:n.*395C=
NM_001272111.2:c.*395C=	NP_001259040.1:n.*395C=
NM_198406.3:c.*663C= MANE Select	NP_940798.1:n.*663C=
NR_073610.2:n.1747C=
NM_001272106.2:c.*395C=	NP_001259035.1:n.*395C=
NM_001272109.2:c.*395C=	NP_001259038.1:n.*395C=
NM_001272112.2:c.*395C=	NP_001259041.1:n.*395C=
NM_001272113.2:c.*395C=	NP_001259042.1:n.*395C=
NM_024897.4:c.*395C=	NP_079173.2:n.*395C=