Canonical Allele Identifier: CA2665216360
Gene: ULK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41883821_41883827del , CM000665.2:g.41883821_41883827del GRCh38
NC_000003.11:g.41925313_41925319del , CM000665.1:g.41925313_41925319del GRCh37
NC_000003.10:g.41900317_41900323del NCBI36
NG_051047.1:g.84198_84204del

Transcript Alleles

HGVS Amino-acid change
ENST00000301831.9:c.1656+51_1656+57del MANE Select ENSP00000301831.4:n.1656+51_1656+57del
ENST00000301831.8:c.1656+51_1656+57del ENSP00000301831.4:n.1656+51_1656+57del
ENST00000420927.5:c.1656+51_1656+57del ENSP00000412187.1:n.1656+51_1656+57del
NM_017886.2:c.1656+51_1656+57del NP_060356.2:n.1656+51_1656+57del
XM_005265261.3:c.1653+51_1653+57del XP_005265318.1:n.1653+51_1653+57del
XM_006713215.2:c.1299+51_1299+57del XP_006713278.1:n.1299+51_1299+57del
XM_011533872.1:c.1656+51_1656+57del XP_011532174.1:n.1656+51_1656+57del
XM_011533873.1:c.1656+51_1656+57del XP_011532175.1:n.1656+51_1656+57del
XM_011533874.1:c.1656+51_1656+57del XP_011532176.1:n.1656+51_1656+57del
XM_011533875.1:c.1656+51_1656+57del XP_011532177.1:n.1656+51_1656+57del
XM_011533876.1:c.1656+51_1656+57del XP_011532178.1:n.1656+51_1656+57del
XM_011533877.1:c.867+51_867+57del XP_011532179.1:n.867+51_867+57del
XM_011533878.1:c.1656+51_1656+57del XP_011532180.1:n.1656+51_1656+57del
XM_011533879.1:c.516+51_516+57del XP_011532181.1:n.516+51_516+57del
XR_427279.2:n.2573+51_2573+57del
NM_001322500.1:c.1656+51_1656+57del NP_001309429.1:n.1656+51_1656+57del
NM_001322501.1:c.750+51_750+57del NP_001309430.1:n.750+51_750+57del
NM_017886.3:c.1656+51_1656+57del NP_060356.2:n.1656+51_1656+57del
NR_136342.1:n.2059+51_2059+57del
NM_017886.4:c.1656+51_1656+57del MANE Select NP_060356.2:n.1656+51_1656+57del
NM_001322500.2:c.1656+51_1656+57del NP_001309429.1:n.1656+51_1656+57del
NM_001322501.2:c.750+51_750+57del NP_001309430.1:n.750+51_750+57del
NR_136342.2:n.1722+51_1722+57del