Canonical Allele Identifier: CA2332838

Gene: ULK4

Linked Data

• ClinVar Variation Id: 403591
• ClinVar RCV Id: RCV000455513
• dbSNP Id: rs2272007
• ExAC: 3:41996136 T / C
• gnomAD v2: 3-41996136-T-C
• gnomAD v3: 3-41954644-T-C
• gnomAD v4: 3-41954644-T-C
• MyVariant Identifiers: chr3:g.41996136T>C (hg19) ; chr3:g.41954644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41954644T>C , CM000665.2:g.41954644T>C	GRCh38
NC_000003.11:g.41996136T>C , CM000665.1:g.41996136T>C	GRCh37
NC_000003.10:g.41971140T>C	NCBI36
NG_051047.1:g.13377A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.116A>G MANE Select	ENSP00000301831.4:p.Lys39Arg
ENST00000301831.8:c.116A>G	ENSP00000301831.4:p.Lys39Arg
ENST00000414606.1:c.116A>G	ENSP00000399382.1:p.Lys39Arg
ENST00000420927.5:c.116A>G	ENSP00000412187.1:p.Lys39Arg
ENST00000431379.5:c.116A>G	ENSP00000391849.1:p.Lys39Arg
ENST00000453224.5:c.116A>G	ENSP00000401414.1:p.Lys39Arg
ENST00000459802.5:n.62+7372A>G
ENST00000460978.1:n.204A>G
ENST00000497684.1:n.155A>G
NM_017886.2:c.116A>G	NP_060356.2:p.Lys39Arg
XM_005265261.3:c.116A>G	XP_005265318.1:p.Lys39Arg
XM_006713215.2:c.-152A>G	XP_006713278.1:n.-152A>G
XM_011533872.1:c.116A>G	XP_011532174.1:p.Lys39Arg
XM_011533873.1:c.116A>G	XP_011532175.1:p.Lys39Arg
XM_011533874.1:c.116A>G	XP_011532176.1:p.Lys39Arg
XM_011533875.1:c.116A>G	XP_011532177.1:p.Lys39Arg
XM_011533876.1:c.116A>G	XP_011532178.1:p.Lys39Arg
XM_011533878.1:c.116A>G	XP_011532180.1:p.Lys39Arg
XR_427279.2:n.1033A>G
NM_001322500.1:c.116A>G	NP_001309429.1:p.Lys39Arg
NM_001322501.1:c.-715A>G	NP_001309430.1:n.-715A>G
NM_017886.3:c.116A>G	NP_060356.2:p.Lys39Arg
NR_136342.1:n.589A>G
NM_017886.4:c.116A>G MANE Select	NP_060356.2:p.Lys39Arg
NM_001322500.2:c.116A>G	NP_001309429.1:p.Lys39Arg
NM_001322501.2:c.-715A>G	NP_001309430.1:n.-715A>G
NR_136342.2:n.252A>G