Canonical Allele Identifier: CA352240481
Gene: ULK4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000301831.9:c.1615T>A MANE Select ENSP00000301831.4:p.Ser539Thr
ENST00000301831.8:c.1615T>A ENSP00000301831.4:p.Ser539Thr
ENST00000420927.5:c.1615T>A ENSP00000412187.1:p.Ser539Thr
NM_017886.2:c.1615T>A NP_060356.2:p.Ser539Thr
XM_005265261.3:c.1612T>A XP_005265318.1:p.Ser538Thr
XM_006713215.2:c.1258T>A XP_006713278.1:p.Ser420Thr
XM_011533872.1:c.1615T>A XP_011532174.1:p.Ser539Thr
XM_011533873.1:c.1615T>A XP_011532175.1:p.Ser539Thr
XM_011533874.1:c.1615T>A XP_011532176.1:p.Ser539Thr
XM_011533875.1:c.1615T>A XP_011532177.1:p.Ser539Thr
XM_011533876.1:c.1615T>A XP_011532178.1:p.Ser539Thr
XM_011533877.1:c.826T>A XP_011532179.1:p.Ser276Thr
XM_011533878.1:c.1615T>A XP_011532180.1:p.Ser539Thr
XM_011533879.1:c.475T>A XP_011532181.1:p.Ser159Thr
XR_427279.2:n.2532T>A
NM_001322500.1:c.1615T>A NP_001309429.1:p.Ser539Thr
NM_001322501.1:c.709T>A NP_001309430.1:p.Ser237Thr
NM_017886.3:c.1615T>A NP_060356.2:p.Ser539Thr
NR_136342.1:n.2018T>A
NM_017886.4:c.1615T>A MANE Select NP_060356.2:p.Ser539Thr
NM_001322500.2:c.1615T>A NP_001309429.1:p.Ser539Thr
NM_001322501.2:c.709T>A NP_001309430.1:p.Ser237Thr
NR_136342.2:n.1681T>A