Canonical Allele Identifier: CA433190823

Gene: ULK4

Linked Data

• dbSNP Id: rs1412192997
• gnomAD v2: 3-41925411-C-T
• gnomAD v3: 3-41883919-C-T
• gnomAD v4: 3-41883919-C-T
• MyVariant Identifiers: chr3:g.41925411C>T (hg19) ; chr3:g.41883919C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883919C>T , CM000665.2:g.41883919C>T	GRCh38
NC_000003.11:g.41925411C>T , CM000665.1:g.41925411C>T	GRCh37
NC_000003.10:g.41900415C>T	NCBI36
NG_051047.1:g.84102G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.1611G>A MANE Select	ENSP00000301831.4:p.Leu537=
ENST00000301831.8:c.1611G>A	ENSP00000301831.4:p.Leu537=
ENST00000420927.5:c.1611G>A	ENSP00000412187.1:p.Leu537=
NM_017886.2:c.1611G>A	NP_060356.2:p.Leu537=
XM_005265261.3:c.1608G>A	XP_005265318.1:p.Leu536=
XM_006713215.2:c.1254G>A	XP_006713278.1:p.Leu418=
XM_011533872.1:c.1611G>A	XP_011532174.1:p.Leu537=
XM_011533873.1:c.1611G>A	XP_011532175.1:p.Leu537=
XM_011533874.1:c.1611G>A	XP_011532176.1:p.Leu537=
XM_011533875.1:c.1611G>A	XP_011532177.1:p.Leu537=
XM_011533876.1:c.1611G>A	XP_011532178.1:p.Leu537=
XM_011533877.1:c.822G>A	XP_011532179.1:p.Leu274=
XM_011533878.1:c.1611G>A	XP_011532180.1:p.Leu537=
XM_011533879.1:c.471G>A	XP_011532181.1:p.Leu157=
XR_427279.2:n.2528G>A
NM_001322500.1:c.1611G>A	NP_001309429.1:p.Leu537=
NM_001322501.1:c.705G>A	NP_001309430.1:p.Leu235=
NM_017886.3:c.1611G>A	NP_060356.2:p.Leu537=
NR_136342.1:n.2014G>A
NM_017886.4:c.1611G>A MANE Select	NP_060356.2:p.Leu537=
NM_001322500.2:c.1611G>A	NP_001309429.1:p.Leu537=
NM_001322501.2:c.705G>A	NP_001309430.1:p.Leu235=
NR_136342.2:n.1677G>A