Canonical Allele Identifier: CA1360083990

Gene: ULK4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883847T= , CM000665.2:g.41883847T=	GRCh38
NC_000003.11:g.41925339T= , CM000665.1:g.41925339T=	GRCh37
NC_000003.10:g.41900343T=	NCBI36
NG_051047.1:g.84174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.1656+27A= MANE Select	ENSP00000301831.4:n.1656+27A=
ENST00000301831.8:c.1656+27A=	ENSP00000301831.4:n.1656+27A=
ENST00000420927.5:c.1656+27A=	ENSP00000412187.1:n.1656+27A=
NM_017886.2:c.1656+27A=	NP_060356.2:n.1656+27A=
XM_005265261.3:c.1653+27A=	XP_005265318.1:n.1653+27A=
XM_006713215.2:c.1299+27A=	XP_006713278.1:n.1299+27A=
XM_011533872.1:c.1656+27A=	XP_011532174.1:n.1656+27A=
XM_011533873.1:c.1656+27A=	XP_011532175.1:n.1656+27A=
XM_011533874.1:c.1656+27A=	XP_011532176.1:n.1656+27A=
XM_011533875.1:c.1656+27A=	XP_011532177.1:n.1656+27A=
XM_011533876.1:c.1656+27A=	XP_011532178.1:n.1656+27A=
XM_011533877.1:c.867+27A=	XP_011532179.1:n.867+27A=
XM_011533878.1:c.1656+27A=	XP_011532180.1:n.1656+27A=
XM_011533879.1:c.516+27A=	XP_011532181.1:n.516+27A=
XR_427279.2:n.2573+27A=
NM_001322500.1:c.1656+27A=	NP_001309429.1:n.1656+27A=
NM_001322501.1:c.750+27A=	NP_001309430.1:n.750+27A=
NM_017886.3:c.1656+27A=	NP_060356.2:n.1656+27A=
NR_136342.1:n.2059+27A=
NM_017886.4:c.1656+27A= MANE Select	NP_060356.2:n.1656+27A=
NM_001322500.2:c.1656+27A=	NP_001309429.1:n.1656+27A=
NM_001322501.2:c.750+27A=	NP_001309430.1:n.750+27A=
NR_136342.2:n.1722+27A=