Canonical Allele Identifier: CA499053434

Gene: ULK2

Linked Data

• MyVariant Identifiers: chr17:g.19700715A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19797402A>C , CM000679.2:g.19797402A>C	GRCh38
NC_000017.10:g.19700715A>C , CM000679.1:g.19700715A>C	GRCh37
NC_000017.9:g.19641307A>C	NCBI36
NG_047113.1:g.75525T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395544.9:c.1803T>G MANE Select	ENSP00000378914.4:p.Pro601=
ENST00000361658.6:c.1803T>G	ENSP00000354877.2:p.Pro601=
ENST00000395544.8:c.1803T>G	ENSP00000378914.4:p.Pro601=
NM_001142610.1:c.1803T>G	NP_001136082.1:p.Pro601=
NM_014683.3:c.1803T>G	NP_055498.3:p.Pro601=
XM_011524087.1:c.1449T>G	XP_011522389.1:p.Pro483=
XR_934124.1:n.2137T>G
XR_934125.1:n.2137T>G
XM_011524087.2:c.1449T>G	XP_011522389.1:p.Pro483=
XM_017025424.2:c.1866T>G	XP_016880913.1:p.Pro622=
XM_017025425.2:c.1866T>G	XP_016880914.1:p.Pro622=
XM_017025426.2:c.1866T>G	XP_016880915.1:p.Pro622=
XM_017025427.2:c.1026T>G	XP_016880916.1:p.Pro342=
XM_017025428.2:c.1026T>G	XP_016880917.1:p.Pro342=
XR_001752700.2:n.2346T>G
XR_001752701.2:n.2346T>G
NM_014683.4:c.1803T>G MANE Select	NP_055498.3:p.Pro601=
NM_001142610.2:c.1803T>G	NP_001136082.1:p.Pro601=