Canonical Allele Identifier: CA8445024

Gene: ULK2

Linked Data

• dbSNP Id: rs776514952
• ExAC: 17:19700692 G / A
• gnomAD v2: 17-19700692-G-A
• gnomAD v4: 17-19797379-G-A
• MyVariant Identifiers: chr17:g.19700692G>A (hg19) ; chr17:g.19797379G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797379G>A , CM000679.2:g.19797379G>A	GRCh38
NC_000017.10:g.19700692G>A , CM000679.1:g.19700692G>A	GRCh37
NC_000017.9:g.19641284G>A	NCBI36
NG_047113.1:g.75548C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395544.9:c.1809+17C>T MANE Select	ENSP00000378914.4:n.1809+17C>T
ENST00000361658.6:c.1809+17C>T	ENSP00000354877.2:n.1809+17C>T
ENST00000395544.8:c.1809+17C>T	ENSP00000378914.4:n.1809+17C>T
NM_001142610.1:c.1809+17C>T	NP_001136082.1:n.1809+17C>T
NM_014683.3:c.1809+17C>T	NP_055498.3:n.1809+17C>T
XM_011524087.1:c.1455+17C>T	XP_011522389.1:n.1455+17C>T
XR_934124.1:n.2143+17C>T
XR_934125.1:n.2143+17C>T
XM_011524087.2:c.1455+17C>T	XP_011522389.1:n.1455+17C>T
XM_017025424.2:c.1872+17C>T	XP_016880913.1:n.1872+17C>T
XM_017025425.2:c.1872+17C>T	XP_016880914.1:n.1872+17C>T
XM_017025426.2:c.1872+17C>T	XP_016880915.1:n.1872+17C>T
XM_017025427.2:c.1032+17C>T	XP_016880916.1:n.1032+17C>T
XM_017025428.2:c.1032+17C>T	XP_016880917.1:n.1032+17C>T
XR_001752700.2:n.2352+17C>T
XR_001752701.2:n.2352+17C>T
NM_014683.4:c.1809+17C>T MANE Select	NP_055498.3:n.1809+17C>T
NM_001142610.2:c.1809+17C>T	NP_001136082.1:n.1809+17C>T