Canonical Allele Identifier: CA352240458

Gene: ULK4

Linked Data

• gnomAD v4: 3-41883910-G-T
• MyVariant Identifiers: chr3:g.41925402G>T (hg19) ; chr3:g.41883910G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883910G>T , CM000665.2:g.41883910G>T	GRCh38
NC_000003.11:g.41925402G>T , CM000665.1:g.41925402G>T	GRCh37
NC_000003.10:g.41900406G>T	NCBI36
NG_051047.1:g.84111C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000301831.9:c.1620C>A MANE Select	ENSP00000301831.4:p.His540Gln
ENST00000301831.8:c.1620C>A	ENSP00000301831.4:p.His540Gln
ENST00000420927.5:c.1620C>A	ENSP00000412187.1:p.His540Gln
NM_017886.2:c.1620C>A	NP_060356.2:p.His540Gln
XM_005265261.3:c.1617C>A	XP_005265318.1:p.His539Gln
XM_006713215.2:c.1263C>A	XP_006713278.1:p.His421Gln
XM_011533872.1:c.1620C>A	XP_011532174.1:p.His540Gln
XM_011533873.1:c.1620C>A	XP_011532175.1:p.His540Gln
XM_011533874.1:c.1620C>A	XP_011532176.1:p.His540Gln
XM_011533875.1:c.1620C>A	XP_011532177.1:p.His540Gln
XM_011533876.1:c.1620C>A	XP_011532178.1:p.His540Gln
XM_011533877.1:c.831C>A	XP_011532179.1:p.His277Gln
XM_011533878.1:c.1620C>A	XP_011532180.1:p.His540Gln
XM_011533879.1:c.480C>A	XP_011532181.1:p.His160Gln
XR_427279.2:n.2537C>A
NM_001322500.1:c.1620C>A	NP_001309429.1:p.His540Gln
NM_001322501.1:c.714C>A	NP_001309430.1:p.His238Gln
NM_017886.3:c.1620C>A	NP_060356.2:p.His540Gln
NR_136342.1:n.2023C>A
NM_017886.4:c.1620C>A MANE Select	NP_060356.2:p.His540Gln
NM_001322500.2:c.1620C>A	NP_001309429.1:p.His540Gln
NM_001322501.2:c.714C>A	NP_001309430.1:p.His238Gln
NR_136342.2:n.1686C>A