Canonical Allele Identifier: CA398720663

Gene: ULK2

Linked Data

• dbSNP Id: rs1060499754
• MyVariant Identifiers: chr17:g.19700785T>A (hg19) ; chr17:g.19797472T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797472T>A , CM000679.2:g.19797472T>A	GRCh38
NC_000017.10:g.19700785T>A , CM000679.1:g.19700785T>A	GRCh37
NC_000017.9:g.19641377T>A	NCBI36
NG_047113.1:g.75455A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395544.9:c.1733A>T MANE Select	ENSP00000378914.4:p.His578Leu
ENST00000361658.6:c.1733A>T	ENSP00000354877.2:p.His578Leu
ENST00000395544.8:c.1733A>T	ENSP00000378914.4:p.His578Leu
NM_001142610.1:c.1733A>T	NP_001136082.1:p.His578Leu
NM_014683.3:c.1733A>T	NP_055498.3:p.His578Leu
XM_011524087.1:c.1379A>T	XP_011522389.1:p.His460Leu
XR_934124.1:n.2067A>T
XR_934125.1:n.2067A>T
XM_011524087.2:c.1379A>T	XP_011522389.1:p.His460Leu
XM_017025424.2:c.1796A>T	XP_016880913.1:p.His599Leu
XM_017025425.2:c.1796A>T	XP_016880914.1:p.His599Leu
XM_017025426.2:c.1796A>T	XP_016880915.1:p.His599Leu
XM_017025427.2:c.956A>T	XP_016880916.1:p.His319Leu
XM_017025428.2:c.956A>T	XP_016880917.1:p.His319Leu
XR_001752700.2:n.2276A>T
XR_001752701.2:n.2276A>T
NM_014683.4:c.1733A>T MANE Select	NP_055498.3:p.His578Leu
NM_001142610.2:c.1733A>T	NP_001136082.1:p.His578Leu