Canonical Allele Identifier: CA1982344078

Gene: P2RY2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73223590C= , CM000673.2:g.73223590C=	GRCh38
NC_000011.9:g.72934635C= , CM000673.1:g.72934635C=	GRCh37
NC_000011.8:g.72612283C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393597.7:c.-199-4391C= MANE Select	ENSP00000377222.2:n.-199-4391C=
ENST00000311131.6:c.-333-4391C=	ENSP00000310305.2:n.-333-4391C=
ENST00000393596.2:c.-199-4391C=	ENSP00000377221.2:n.-199-4391C=
ENST00000393597.6:c.-199-4391C=	ENSP00000377222.2:n.-199-4391C=
NM_002564.3:c.-199-4391C=	NP_002555.3:n.-199-4391C=
NM_176071.2:c.-199-4391C=	NP_788085.2:n.-199-4391C=
NM_176072.2:c.-333-4391C=	NP_788086.2:n.-333-4391C=
XM_005274019.3:c.-199-4391C=	XP_005274076.1:n.-199-4391C=
XM_005274020.3:c.-200+2971C=	XP_005274077.1:n.-200+2971C=
XM_005274021.3:c.-199-4391C=	XP_005274078.1:n.-199-4391C=
XM_011545074.1:c.-199-4391C=	XP_011543376.1:n.-199-4391C=
XM_005274019.4:c.-199-4391C=	XP_005274076.1:n.-199-4391C=
XM_005274020.4:c.-200+2971C=	XP_005274077.1:n.-200+2971C=
XM_005274021.4:c.-199-4391C=	XP_005274078.1:n.-199-4391C=
XM_011545074.2:c.-199-4391C=	XP_011543376.1:n.-199-4391C=
XM_017017839.1:c.-199-4391C=	XP_016873328.1:n.-199-4391C=
XR_001747890.1:n.154-4391C=
XR_001747891.1:n.154-4391C=
XR_001747892.1:n.154-4391C=
NM_002564.4:c.-199-4391C= MANE Select	NP_002555.4:n.-199-4391C=
NM_176071.3:c.-199-4391C=	NP_788085.3:n.-199-4391C=
NM_176072.3:c.-333-4391C=	NP_788086.3:n.-333-4391C=