Canonical Allele Identifier: CA398720491

Gene: ULK2

Linked Data

• MyVariant Identifiers: chr17:g.19700708C>A (hg19) ; chr17:g.19797395C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797395C>A , CM000679.2:g.19797395C>A	GRCh38
NC_000017.10:g.19700708C>A , CM000679.1:g.19700708C>A	GRCh37
NC_000017.9:g.19641300C>A	NCBI36
NG_047113.1:g.75532G>T

Transcript Alleles

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