Canonical Allele Identifier: CA1360059727

Gene: ULK4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41835922T= , CM000665.2:g.41835922T=	GRCh38
NC_000003.11:g.41877414T= , CM000665.1:g.41877414T=	GRCh37
NC_000003.10:g.41852418T=	NCBI36
NG_051047.1:g.132099A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.1706A= MANE Select	ENSP00000301831.4:p.Lys569=
ENST00000301831.8:c.1706A=	ENSP00000301831.4:p.Lys569=
ENST00000460406.1:n.187A=
NM_017886.2:c.1706A=	NP_060356.2:p.Lys569=
XM_005265261.3:c.1703A=	XP_005265318.1:p.Lys568=
XM_006713215.2:c.1349A=	XP_006713278.1:p.Lys450=
XM_011533872.1:c.1706A=	XP_011532174.1:p.Lys569=
XM_011533873.1:c.1706A=	XP_011532175.1:p.Lys569=
XM_011533874.1:c.1706A=	XP_011532176.1:p.Lys569=
XM_011533875.1:c.1706A=	XP_011532177.1:p.Lys569=
XM_011533876.1:c.1706A=	XP_011532178.1:p.Lys569=
XM_011533877.1:c.917A=	XP_011532179.1:p.Lys306=
XM_011533878.1:c.1706A=	XP_011532180.1:p.Lys569=
XM_011533879.1:c.566A=	XP_011532181.1:p.Lys189=
XM_011533880.1:c.-122A=	XP_011532182.1:n.-122A=
XR_427279.2:n.2623A=
NM_001322500.1:c.1706A=	NP_001309429.1:p.Lys569=
NM_001322501.1:c.800A=	NP_001309430.1:p.Lys267=
NM_017886.3:c.1706A=	NP_060356.2:p.Lys569=
NR_136342.1:n.2109A=
XM_011533880.3:c.-122A=	XP_011532182.1:n.-122A=
XM_024453612.1:c.-80A=	XP_024309380.1:n.-80A=
XM_024453613.1:c.-122A=	XP_024309381.1:n.-122A=
NM_017886.4:c.1706A= MANE Select	NP_060356.2:p.Lys569=
NM_001322500.2:c.1706A=	NP_001309429.1:p.Lys569=
NM_001322501.2:c.800A=	NP_001309430.1:p.Lys267=
NR_136342.2:n.1772A=