Canonical Allele Identifier: CA352240492

Gene: ULK4

Linked Data

• MyVariant Identifiers: chr3:g.41925412A>C (hg19) ; chr3:g.41883920A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883920A>C , CM000665.2:g.41883920A>C	GRCh38
NC_000003.11:g.41925412A>C , CM000665.1:g.41925412A>C	GRCh37
NC_000003.10:g.41900416A>C	NCBI36
NG_051047.1:g.84101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.1610T>G MANE Select	ENSP00000301831.4:p.Leu537Arg
ENST00000301831.8:c.1610T>G	ENSP00000301831.4:p.Leu537Arg
ENST00000420927.5:c.1610T>G	ENSP00000412187.1:p.Leu537Arg
NM_017886.2:c.1610T>G	NP_060356.2:p.Leu537Arg
XM_005265261.3:c.1607T>G	XP_005265318.1:p.Leu536Arg
XM_006713215.2:c.1253T>G	XP_006713278.1:p.Leu418Arg
XM_011533872.1:c.1610T>G	XP_011532174.1:p.Leu537Arg
XM_011533873.1:c.1610T>G	XP_011532175.1:p.Leu537Arg
XM_011533874.1:c.1610T>G	XP_011532176.1:p.Leu537Arg
XM_011533875.1:c.1610T>G	XP_011532177.1:p.Leu537Arg
XM_011533876.1:c.1610T>G	XP_011532178.1:p.Leu537Arg
XM_011533877.1:c.821T>G	XP_011532179.1:p.Leu274Arg
XM_011533878.1:c.1610T>G	XP_011532180.1:p.Leu537Arg
XM_011533879.1:c.470T>G	XP_011532181.1:p.Leu157Arg
XR_427279.2:n.2527T>G
NM_001322500.1:c.1610T>G	NP_001309429.1:p.Leu537Arg
NM_001322501.1:c.704T>G	NP_001309430.1:p.Leu235Arg
NM_017886.3:c.1610T>G	NP_060356.2:p.Leu537Arg
NR_136342.1:n.2013T>G
NM_017886.4:c.1610T>G MANE Select	NP_060356.2:p.Leu537Arg
NM_001322500.2:c.1610T>G	NP_001309429.1:p.Leu537Arg
NM_001322501.2:c.704T>G	NP_001309430.1:p.Leu235Arg
NR_136342.2:n.1676T>G