Canonical Allele Identifier: CA625320343

Gene: ULK2

Linked Data

• dbSNP Id: rs1265243907
• gnomAD v2: 17-19700706-A-C
• gnomAD v4: 17-19797393-A-C
• MyVariant Identifiers: chr17:g.19700706A>C (hg19) ; chr17:g.19797393A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797393A>C , CM000679.2:g.19797393A>C	GRCh38
NC_000017.10:g.19700706A>C , CM000679.1:g.19700706A>C	GRCh37
NC_000017.9:g.19641298A>C	NCBI36
NG_047113.1:g.75534T>G

Transcript Alleles

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