Canonical Allele Identifier: CA387296051
Gene: ULK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131919544C>A , CM000674.2:g.131919544C>A GRCh38
NC_000012.11:g.132404089C>A , CM000674.1:g.132404089C>A GRCh37
NC_000012.10:g.130970042C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321867.6:c.2757C>A MANE Select ENSP00000324560.3:p.Asp919Glu
ENST00000321867.5:c.2757C>A ENSP00000324560.3:p.Asp919Glu
ENST00000540647.5:n.626C>A
ENST00000544718.1:n.304C>A
NM_003565.2:c.2757C>A NP_003556.1:p.Asp919Glu
XM_011538798.1:c.2826C>A XP_011537100.1:p.Asp942Glu
XM_011538799.1:c.2739C>A XP_011537101.1:p.Asp913Glu
XR_944753.1:n.2539C>A
XM_011538798.3:c.2826C>A XP_011537100.1:p.Asp942Glu
XM_011538799.2:c.2739C>A XP_011537101.1:p.Asp913Glu
XR_001748883.2:n.2545C>A
NM_003565.3:c.2757C>A NP_003556.1:p.Asp919Glu
NM_003565.4:c.2757C>A MANE Select NP_003556.2:p.Asp919Glu