Canonical Allele Identifier: CA352240478

Gene: ULK4

Linked Data

• MyVariant Identifiers: chr3:g.41925407A>C (hg19) ; chr3:g.41883915A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883915A>C , CM000665.2:g.41883915A>C	GRCh38
NC_000003.11:g.41925407A>C , CM000665.1:g.41925407A>C	GRCh37
NC_000003.10:g.41900411A>C	NCBI36
NG_051047.1:g.84106T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301831.9:c.1615T>G MANE Select	ENSP00000301831.4:p.Ser539Ala
ENST00000301831.8:c.1615T>G	ENSP00000301831.4:p.Ser539Ala
ENST00000420927.5:c.1615T>G	ENSP00000412187.1:p.Ser539Ala
NM_017886.2:c.1615T>G	NP_060356.2:p.Ser539Ala
XM_005265261.3:c.1612T>G	XP_005265318.1:p.Ser538Ala
XM_006713215.2:c.1258T>G	XP_006713278.1:p.Ser420Ala
XM_011533872.1:c.1615T>G	XP_011532174.1:p.Ser539Ala
XM_011533873.1:c.1615T>G	XP_011532175.1:p.Ser539Ala
XM_011533874.1:c.1615T>G	XP_011532176.1:p.Ser539Ala
XM_011533875.1:c.1615T>G	XP_011532177.1:p.Ser539Ala
XM_011533876.1:c.1615T>G	XP_011532178.1:p.Ser539Ala
XM_011533877.1:c.826T>G	XP_011532179.1:p.Ser276Ala
XM_011533878.1:c.1615T>G	XP_011532180.1:p.Ser539Ala
XM_011533879.1:c.475T>G	XP_011532181.1:p.Ser159Ala
XR_427279.2:n.2532T>G
NM_001322500.1:c.1615T>G	NP_001309429.1:p.Ser539Ala
NM_001322501.1:c.709T>G	NP_001309430.1:p.Ser237Ala
NM_017886.3:c.1615T>G	NP_060356.2:p.Ser539Ala
NR_136342.1:n.2018T>G
NM_017886.4:c.1615T>G MANE Select	NP_060356.2:p.Ser539Ala
NM_001322500.2:c.1615T>G	NP_001309429.1:p.Ser539Ala
NM_001322501.2:c.709T>G	NP_001309430.1:p.Ser237Ala
NR_136342.2:n.1681T>G