Canonical Allele Identifier: CA352240466

Gene: ULK4

Linked Data

• dbSNP Id: rs1697619957
• MyVariant Identifiers: chr3:g.41925403T>C (hg19) ; chr3:g.41883911T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883911T>C , CM000665.2:g.41883911T>C	GRCh38
NC_000003.11:g.41925403T>C , CM000665.1:g.41925403T>C	GRCh37
NC_000003.10:g.41900407T>C	NCBI36
NG_051047.1:g.84110A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301831.9:c.1619A>G MANE Select	ENSP00000301831.4:p.His540Arg
ENST00000301831.8:c.1619A>G	ENSP00000301831.4:p.His540Arg
ENST00000420927.5:c.1619A>G	ENSP00000412187.1:p.His540Arg
NM_017886.2:c.1619A>G	NP_060356.2:p.His540Arg
XM_005265261.3:c.1616A>G	XP_005265318.1:p.His539Arg
XM_006713215.2:c.1262A>G	XP_006713278.1:p.His421Arg
XM_011533872.1:c.1619A>G	XP_011532174.1:p.His540Arg
XM_011533873.1:c.1619A>G	XP_011532175.1:p.His540Arg
XM_011533874.1:c.1619A>G	XP_011532176.1:p.His540Arg
XM_011533875.1:c.1619A>G	XP_011532177.1:p.His540Arg
XM_011533876.1:c.1619A>G	XP_011532178.1:p.His540Arg
XM_011533877.1:c.830A>G	XP_011532179.1:p.His277Arg
XM_011533878.1:c.1619A>G	XP_011532180.1:p.His540Arg
XM_011533879.1:c.479A>G	XP_011532181.1:p.His160Arg
XR_427279.2:n.2536A>G
NM_001322500.1:c.1619A>G	NP_001309429.1:p.His540Arg
NM_001322501.1:c.713A>G	NP_001309430.1:p.His238Arg
NM_017886.3:c.1619A>G	NP_060356.2:p.His540Arg
NR_136342.1:n.2022A>G
NM_017886.4:c.1619A>G MANE Select	NP_060356.2:p.His540Arg
NM_001322500.2:c.1619A>G	NP_001309429.1:p.His540Arg
NM_001322501.2:c.713A>G	NP_001309430.1:p.His238Arg
NR_136342.2:n.1685A>G