Canonical Allele Identifier: CA2332268

Gene: ULK4

Linked Data

• ClinVar Variation Id: 403586
• ClinVar RCV Id: RCV000455999
• dbSNP Id: rs1717003
• ExAC: 3:41937000 C / T
• gnomAD v2: 3-41937000-C-T
• gnomAD v3: 3-41895508-C-T
• gnomAD v4: 3-41895508-C-T
• MyVariant Identifiers: chr3:g.41937000C>T (hg19) ; chr3:g.41895508C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41895508C>T , CM000665.2:g.41895508C>T	GRCh38
NC_000003.11:g.41937000C>T , CM000665.1:g.41937000C>T	GRCh37
NC_000003.10:g.41912004C>T	NCBI36
NG_051047.1:g.72513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.1577+10G>A MANE Select	ENSP00000301831.4:n.1577+10G>A
ENST00000301831.8:c.1577+10G>A	ENSP00000301831.4:n.1577+10G>A
ENST00000420927.5:c.1577+10G>A	ENSP00000412187.1:n.1577+10G>A
NM_017886.2:c.1577+10G>A	NP_060356.2:n.1577+10G>A
XM_005265261.3:c.1574+10G>A	XP_005265318.1:n.1574+10G>A
XM_006713215.2:c.1220+10G>A	XP_006713278.1:n.1220+10G>A
XM_011533872.1:c.1577+10G>A	XP_011532174.1:n.1577+10G>A
XM_011533873.1:c.1577+10G>A	XP_011532175.1:n.1577+10G>A
XM_011533874.1:c.1577+10G>A	XP_011532176.1:n.1577+10G>A
XM_011533875.1:c.1577+10G>A	XP_011532177.1:n.1577+10G>A
XM_011533876.1:c.1577+10G>A	XP_011532178.1:n.1577+10G>A
XM_011533877.1:c.788+10G>A	XP_011532179.1:n.788+10G>A
XM_011533878.1:c.1577+10G>A	XP_011532180.1:n.1577+10G>A
XM_011533879.1:c.437+10G>A	XP_011532181.1:n.437+10G>A
XR_427279.2:n.2494+10G>A
NM_001322500.1:c.1577+10G>A	NP_001309429.1:n.1577+10G>A
NM_001322501.1:c.671+10G>A	NP_001309430.1:n.671+10G>A
NM_017886.3:c.1577+10G>A	NP_060356.2:n.1577+10G>A
NR_136342.1:n.1980+10G>A
NM_017886.4:c.1577+10G>A MANE Select	NP_060356.2:n.1577+10G>A
NM_001322500.2:c.1577+10G>A	NP_001309429.1:n.1577+10G>A
NM_001322501.2:c.671+10G>A	NP_001309430.1:n.671+10G>A
NR_136342.2:n.1643+10G>A