Canonical Allele Identifier: CA2332234
Gene: ULK4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 403584
ClinVar RCV Id: RCV000454745
dbSNP Id: rs1052501

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41883906C>T , CM000665.2:g.41883906C>T GRCh38
NC_000003.11:g.41925398C>T , CM000665.1:g.41925398C>T GRCh37
NC_000003.10:g.41900402C>T NCBI36
NG_051047.1:g.84115G>A

Transcript Alleles

HGVS Amino-acid change
NM_017886.2:c.1624G>A VV NP_060356.2:p.Ala542Thr
XM_005265261.3:c.1621G>A XP_005265318.1:p.Ala541Thr
XM_006713215.2:c.1267G>A XP_006713278.1:p.Ala423Thr
XM_011533872.1:c.1624G>A XP_011532174.1:p.Ala542Thr
XM_011533873.1:c.1624G>A XP_011532175.1:p.Ala542Thr
XM_011533874.1:c.1624G>A XP_011532176.1:p.Ala542Thr
XM_011533875.1:c.1624G>A XP_011532177.1:p.Ala542Thr
XM_011533876.1:c.1624G>A XP_011532178.1:p.Ala542Thr
XM_011533877.1:c.835G>A XP_011532179.1:p.Ala279Thr
XM_011533878.1:c.1624G>A XP_011532180.1:p.Ala542Thr
XM_011533879.1:c.484G>A XP_011532181.1:p.Ala162Thr
XR_427279.2:n.2541G>A
NM_001322500.1:c.1624G>A VV NP_001309429.1:p.Ala542Thr
NM_001322501.1:c.718G>A VV NP_001309430.1:p.Ala240Thr
NM_017886.3:c.1624G>A VV
NR_136342.1:n.2027G>A
NM_017886.4:c.1624G>A VV MANE Preferred
ENST00000301831.8:c.1624G>A ENSP00000301831.4:p.Ala542Thr
ENST00000420927.5:c.1624G>A ENSP00000412187.1:p.Ala542Thr