Canonical Allele Identifier: CA2665216389

Gene: ULK4

Linked Data

• gnomAD v4: 3-41883919-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883920del , CM000665.2:g.41883920del	GRCh38
NC_000003.11:g.41925412del , CM000665.1:g.41925412del	GRCh37
NC_000003.10:g.41900416del	NCBI36
NG_051047.1:g.84101del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301831.9:c.1610del MANE Select	ENSP00000301831.4:p.Leu537ArgfsTer21
ENST00000301831.8:c.1610del	ENSP00000301831.4:p.Leu537ArgfsTer21
ENST00000420927.5:c.1610del	ENSP00000412187.1:p.Leu537ArgfsTer26
NM_017886.2:c.1610del	NP_060356.2:p.Leu537ArgfsTer21
XM_005265261.3:c.1607del	XP_005265318.1:p.Leu536ArgfsTer21
XM_006713215.2:c.1253del	XP_006713278.1:p.Leu418ArgfsTer21
XM_011533872.1:c.1610del	XP_011532174.1:p.Leu537ArgfsTer21
XM_011533873.1:c.1610del	XP_011532175.1:p.Leu537ArgfsTer21
XM_011533874.1:c.1610del	XP_011532176.1:p.Leu537ArgfsTer21
XM_011533875.1:c.1610del	XP_011532177.1:p.Leu537ArgfsTer21
XM_011533876.1:c.1610del	XP_011532178.1:p.Leu537ArgfsTer21
XM_011533877.1:c.821del	XP_011532179.1:p.Leu274ArgfsTer21
XM_011533878.1:c.1610del	XP_011532180.1:p.Leu537ArgfsTer21
XM_011533879.1:c.470del	XP_011532181.1:p.Leu157ArgfsTer21
XR_427279.2:n.2527del
NM_001322500.1:c.1610del	NP_001309429.1:p.Leu537ArgfsTer21
NM_001322501.1:c.704del	NP_001309430.1:p.Leu235ArgfsTer21
NM_017886.3:c.1610del	NP_060356.2:p.Leu537ArgfsTer21
NR_136342.1:n.2013del
NM_017886.4:c.1610del MANE Select	NP_060356.2:p.Leu537ArgfsTer21
NM_001322500.2:c.1610del	NP_001309429.1:p.Leu537ArgfsTer21
NM_001322501.2:c.704del	NP_001309430.1:p.Leu235ArgfsTer21
NR_136342.2:n.1676del