Canonical Allele Identifier: CA2251212822

Gene: ULK2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797381G= , CM000679.2:g.19797381G=	GRCh38
NC_000017.10:g.19700694G= , CM000679.1:g.19700694G=	GRCh37
NC_000017.9:g.19641286G=	NCBI36
NG_047113.1:g.75546C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395544.9:c.1809+15C= MANE Select	ENSP00000378914.4:n.1809+15C=
ENST00000361658.6:c.1809+15C=	ENSP00000354877.2:n.1809+15C=
ENST00000395544.8:c.1809+15C=	ENSP00000378914.4:n.1809+15C=
NM_001142610.1:c.1809+15C=	NP_001136082.1:n.1809+15C=
NM_014683.3:c.1809+15C=	NP_055498.3:n.1809+15C=
XM_011524087.1:c.1455+15C=	XP_011522389.1:n.1455+15C=
XR_934124.1:n.2143+15C=
XR_934125.1:n.2143+15C=
XM_011524087.2:c.1455+15C=	XP_011522389.1:n.1455+15C=
XM_017025424.2:c.1872+15C=	XP_016880913.1:n.1872+15C=
XM_017025425.2:c.1872+15C=	XP_016880914.1:n.1872+15C=
XM_017025426.2:c.1872+15C=	XP_016880915.1:n.1872+15C=
XM_017025427.2:c.1032+15C=	XP_016880916.1:n.1032+15C=
XM_017025428.2:c.1032+15C=	XP_016880917.1:n.1032+15C=
XR_001752700.2:n.2352+15C=
XR_001752701.2:n.2352+15C=
NM_014683.4:c.1809+15C= MANE Select	NP_055498.3:n.1809+15C=
NM_001142610.2:c.1809+15C=	NP_001136082.1:n.1809+15C=