Canonical Allele Identifier: CA2332153

Gene: ULK4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_017886.4:c.1706A>G MANE Select	NP_060356.2:p.Lys569Arg
ENST00000301831.9:c.1706A>G MANE Select	ENSP00000301831.4:p.Lys569Arg
NM_001322500.1:c.1706A>G	NP_001309429.1:p.Lys569Arg
NM_001322500.2:c.1706A>G	NP_001309429.1:p.Lys569Arg
NM_001322501.1:c.800A>G	NP_001309430.1:p.Lys267Arg
NM_001322501.2:c.800A>G	NP_001309430.1:p.Lys267Arg
NM_017886.2:c.1706A>G	NP_060356.2:p.Lys569Arg
NM_017886.3:c.1706A>G	NP_060356.2:p.Lys569Arg
NR_136342.1:n.2109A>G
NR_136342.2:n.1772A>G
ENST00000301831.8:c.1706A>G	ENSP00000301831.4:p.Lys569Arg
ENST00000460406.1:n.187A>G
XM_005265261.3:c.1703A>G	XP_005265318.1:p.Lys568Arg
XM_006713215.2:c.1349A>G	XP_006713278.1:p.Lys450Arg
XM_011533872.1:c.1706A>G	XP_011532174.1:p.Lys569Arg
XM_011533873.1:c.1706A>G	XP_011532175.1:p.Lys569Arg
XM_011533874.1:c.1706A>G	XP_011532176.1:p.Lys569Arg
XM_011533875.1:c.1706A>G	XP_011532177.1:p.Lys569Arg
XM_011533876.1:c.1706A>G	XP_011532178.1:p.Lys569Arg
XM_011533877.1:c.917A>G	XP_011532179.1:p.Lys306Arg
XM_011533878.1:c.1706A>G	XP_011532180.1:p.Lys569Arg
XM_011533879.1:c.566A>G	XP_011532181.1:p.Lys189Arg
XM_011533880.1:c.-122A>G	XP_011532182.1:n.-122A>G
XM_011533880.3:c.-122A>G	XP_011532182.1:n.-122A>G
XM_024453612.1:c.-80A>G	XP_024309380.1:n.-80A>G
XM_024453613.1:c.-122A>G	XP_024309381.1:n.-122A>G
XR_427279.2:n.2623A>G