Canonical Allele Identifier: CA2404640683

Gene: PICK1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.38059462T= , CM000684.2:g.38059462T=	GRCh38
NC_000022.10:g.38455469T= , CM000684.1:g.38455469T=	GRCh37
NC_000022.9:g.36785415T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012407.4:c.153+117T= MANE Select	NP_036539.1:n.153+117T=
ENST00000356976.8:c.153+117T= MANE Select	ENSP00000349465.3:n.153+117T=
NM_001039583.1:c.153+117T=	NP_001034672.1:n.153+117T=
NM_001039584.1:c.153+117T=	NP_001034673.1:n.153+117T=
NM_012407.3:c.153+117T=	NP_036539.1:n.153+117T=
ENST00000356976.7:c.153+117T=	ENSP00000349465.3:n.153+117T=
ENST00000404072.7:c.153+117T=	ENSP00000385205.3:n.153+117T=
ENST00000424694.5:c.153+117T=	ENSP00000398141.1:n.153+117T=
ENST00000426258.5:c.41+1612T=	ENSP00000413962.1:n.41+1612T=
ENST00000432756.6:c.41+1612T=	ENSP00000387861.2:n.41+1612T=
ENST00000435166.1:c.153+117T=	ENSP00000397588.1:n.153+117T=
ENST00000437453.5:c.153+117T=	ENSP00000410793.1:n.153+117T=
ENST00000466374.1:n.315+117T=
ENST00000468288.5:n.229+117T=
ENST00000469819.5:n.391+117T=
ENST00000484021.5:n.392+117T=
XM_006724379.1:c.-165+117T=	XP_006724442.1:n.-165+117T=
XM_006724379.2:c.-165+117T=	XP_006724442.1:n.-165+117T=
XM_006724380.1:c.-165+117T=	XP_006724443.1:n.-165+117T=
XM_006724380.2:c.-165+117T=	XP_006724443.1:n.-165+117T=
XM_011530517.1:c.153+117T=	XP_011528819.1:n.153+117T=
XM_011530517.3:c.153+117T=	XP_011528819.1:n.153+117T=
XM_017029090.1:c.-274+1612T=	XP_016884579.1:n.-274+1612T=
XM_017029091.1:c.-112+1612T=	XP_016884580.1:n.-112+1612T=
XM_017029092.1:c.-274+117T=	XP_016884581.1:n.-274+117T=
XM_017029093.1:c.-165+1612T=	XP_016884582.1:n.-165+1612T=
XM_017029094.1:c.-165+1612T=	XP_016884583.1:n.-165+1612T=
XR_002958723.1:n.304+117T=
XR_002958724.1:n.396+117T=
XR_002958725.1:n.298+117T=
XR_002958726.1:n.670+117T=
XR_002958727.1:n.670+117T=
XR_937962.1:n.614+117T=