Canonical Allele Identifier: CA288577634

Gene: ULK2

Linked Data

• dbSNP Id: rs895414975
• gnomAD v2: 17-19700714-T-A
• gnomAD v4: 17-19797401-T-A
• MyVariant Identifiers: chr17:g.19700714T>A (hg19) ; chr17:g.19797401T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797401T>A , CM000679.2:g.19797401T>A	GRCh38
NC_000017.10:g.19700714T>A , CM000679.1:g.19700714T>A	GRCh37
NC_000017.9:g.19641306T>A	NCBI36
NG_047113.1:g.75526A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395544.9:c.1804A>T MANE Select	ENSP00000378914.4:p.Thr602Ser
ENST00000361658.6:c.1804A>T	ENSP00000354877.2:p.Thr602Ser
ENST00000395544.8:c.1804A>T	ENSP00000378914.4:p.Thr602Ser
NM_001142610.1:c.1804A>T	NP_001136082.1:p.Thr602Ser
NM_014683.3:c.1804A>T	NP_055498.3:p.Thr602Ser
XM_011524087.1:c.1450A>T	XP_011522389.1:p.Thr484Ser
XR_934124.1:n.2138A>T
XR_934125.1:n.2138A>T
XM_011524087.2:c.1450A>T	XP_011522389.1:p.Thr484Ser
XM_017025424.2:c.1867A>T	XP_016880913.1:p.Thr623Ser
XM_017025425.2:c.1867A>T	XP_016880914.1:p.Thr623Ser
XM_017025426.2:c.1867A>T	XP_016880915.1:p.Thr623Ser
XM_017025427.2:c.1027A>T	XP_016880916.1:p.Thr343Ser
XM_017025428.2:c.1027A>T	XP_016880917.1:p.Thr343Ser
XR_001752700.2:n.2347A>T
XR_001752701.2:n.2347A>T
NM_014683.4:c.1804A>T MANE Select	NP_055498.3:p.Thr602Ser
NM_001142610.2:c.1804A>T	NP_001136082.1:p.Thr602Ser