Canonical Allele Identifier: CA2251212827

Gene: ULK2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797399A= , CM000679.2:g.19797399A=	GRCh38
NC_000017.10:g.19700712A= , CM000679.1:g.19700712A=	GRCh37
NC_000017.9:g.19641304A=	NCBI36
NG_047113.1:g.75528T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395544.9:c.1806T= MANE Select	ENSP00000378914.4:p.Thr602=
ENST00000361658.6:c.1806T=	ENSP00000354877.2:p.Thr602=
ENST00000395544.8:c.1806T=	ENSP00000378914.4:p.Thr602=
NM_001142610.1:c.1806T=	NP_001136082.1:p.Thr602=
NM_014683.3:c.1806T=	NP_055498.3:p.Thr602=
XM_011524087.1:c.1452T=	XP_011522389.1:p.Thr484=
XR_934124.1:n.2140T=
XR_934125.1:n.2140T=
XM_011524087.2:c.1452T=	XP_011522389.1:p.Thr484=
XM_017025424.2:c.1869T=	XP_016880913.1:p.Thr623=
XM_017025425.2:c.1869T=	XP_016880914.1:p.Thr623=
XM_017025426.2:c.1869T=	XP_016880915.1:p.Thr623=
XM_017025427.2:c.1029T=	XP_016880916.1:p.Thr343=
XM_017025428.2:c.1029T=	XP_016880917.1:p.Thr343=
XR_001752700.2:n.2349T=
XR_001752701.2:n.2349T=
NM_014683.4:c.1806T= MANE Select	NP_055498.3:p.Thr602=
NM_001142610.2:c.1806T=	NP_001136082.1:p.Thr602=