Canonical Allele Identifier: CA1360010989

Gene: ULK4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41744517T= , CM000665.2:g.41744517T=	GRCh38
NC_000003.11:g.41786009T= , CM000665.1:g.41786009T=	GRCh37
NC_000003.10:g.41761013T=	NCBI36
NG_051047.1:g.223504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.2321+9844A= MANE Select	ENSP00000301831.4:n.2321+9844A=
ENST00000301831.8:c.2321+9844A=	ENSP00000301831.4:n.2321+9844A=
NM_017886.2:c.2321+9844A=	NP_060356.2:n.2321+9844A=
XM_005265261.3:c.2318+9844A=	XP_005265318.1:n.2318+9844A=
XM_006713215.2:c.1964+9844A=	XP_006713278.1:n.1964+9844A=
XM_011533872.1:c.2321+9844A=	XP_011532174.1:n.2321+9844A=
XM_011533873.1:c.2321+9844A=	XP_011532175.1:n.2321+9844A=
XM_011533874.1:c.2321+9844A=	XP_011532176.1:n.2321+9844A=
XM_011533875.1:c.2321+9844A=	XP_011532177.1:n.2321+9844A=
XM_011533876.1:c.2321+9844A=	XP_011532178.1:n.2321+9844A=
XM_011533877.1:c.1532+9844A=	XP_011532179.1:n.1532+9844A=
XM_011533878.1:c.2321+9844A=	XP_011532180.1:n.2321+9844A=
XM_011533879.1:c.1181+9844A=	XP_011532181.1:n.1181+9844A=
XM_011533880.1:c.494+9844A=	XP_011532182.1:n.494+9844A=
XR_427279.2:n.3111-26656A=
NM_001322500.1:c.2321+9844A=	NP_001309429.1:n.2321+9844A=
NM_001322501.1:c.1415+9844A=	NP_001309430.1:n.1415+9844A=
NM_017886.3:c.2321+9844A=	NP_060356.2:n.2321+9844A=
NR_136342.1:n.2724+9844A=
XM_011533880.3:c.494+9844A=	XP_011532182.1:n.494+9844A=
XM_024453612.1:c.452+9844A=	XP_024309380.1:n.452+9844A=
XM_024453613.1:c.494+9844A=	XP_024309381.1:n.494+9844A=
NM_017886.4:c.2321+9844A= MANE Select	NP_060356.2:n.2321+9844A=
NM_001322500.2:c.2321+9844A=	NP_001309429.1:n.2321+9844A=
NM_001322501.2:c.1415+9844A=	NP_001309430.1:n.1415+9844A=
NR_136342.2:n.2387+9844A=