Canonical Allele Identifier: CA358644

Gene: ULK4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41715287G>A , CM000665.2:g.41715287G>A	GRCh38
NC_000003.11:g.41756779G>A , CM000665.1:g.41756779G>A	GRCh37
NC_000003.10:g.41731783G>A	NCBI36
NG_051047.1:g.252734C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017886.4:c.2584C>T MANE Select	NP_060356.2:p.Arg862Ter
ENST00000301831.9:c.2584C>T MANE Select	ENSP00000301831.4:p.Arg862Ter
NM_001322500.1:c.2584C>T	NP_001309429.1:p.Arg862Ter
NM_001322500.2:c.2584C>T	NP_001309429.1:p.Arg862Ter
NM_001322501.1:c.1678C>T	NP_001309430.1:p.Arg560Ter
NM_001322501.2:c.1678C>T	NP_001309430.1:p.Arg560Ter
NM_017886.2:c.2584C>T	NP_060356.2:p.Arg862Ter
NM_017886.3:c.2584C>T	NP_060356.2:p.Arg862Ter
NR_136342.1:n.2987C>T
NR_136342.2:n.2650C>T
ENST00000301831.8:c.2584C>T	ENSP00000301831.4:p.Arg862Ter
XM_005265261.3:c.2581C>T	XP_005265318.1:p.Arg861Ter
XM_006713215.2:c.2227C>T	XP_006713278.1:p.Arg743Ter
XM_011533872.1:c.2584C>T	XP_011532174.1:p.Arg862Ter
XM_011533873.1:c.2584C>T	XP_011532175.1:p.Arg862Ter
XM_011533874.1:c.2584C>T	XP_011532176.1:p.Arg862Ter
XM_011533875.1:c.2584C>T	XP_011532177.1:p.Arg862Ter
XM_011533876.1:c.2584C>T	XP_011532178.1:p.Arg862Ter
XM_011533877.1:c.1795C>T	XP_011532179.1:p.Arg599Ter
XM_011533878.1:c.2584C>T	XP_011532180.1:p.Arg862Ter
XM_011533879.1:c.1444C>T	XP_011532181.1:p.Arg482Ter
XM_011533880.1:c.757C>T	XP_011532182.1:p.Arg253Ter
XM_011533880.3:c.757C>T	XP_011532182.1:p.Arg253Ter
XM_024453612.1:c.715C>T	XP_024309380.1:p.Arg239Ter
XM_024453613.1:c.757C>T	XP_024309381.1:p.Arg253Ter
XR_427279.2:n.3373C>T