Canonical Allele Identifier: CA433190825
Gene: ULK4 HGNC NCBI

Linked Data

dbSNP Id: rs1432974073
gnomAD v4: 3-41883921-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41883921G>A , CM000665.2:g.41883921G>A GRCh38
NC_000003.11:g.41925413G>A , CM000665.1:g.41925413G>A GRCh37
NC_000003.10:g.41900417G>A NCBI36
NG_051047.1:g.84100C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301831.9:c.1609C>T MANE Select ENSP00000301831.4:p.Leu537=
ENST00000301831.8:c.1609C>T ENSP00000301831.4:p.Leu537=
ENST00000420927.5:c.1609C>T ENSP00000412187.1:p.Leu537=
NM_017886.2:c.1609C>T NP_060356.2:p.Leu537=
XM_005265261.3:c.1606C>T XP_005265318.1:p.Leu536=
XM_006713215.2:c.1252C>T XP_006713278.1:p.Leu418=
XM_011533872.1:c.1609C>T XP_011532174.1:p.Leu537=
XM_011533873.1:c.1609C>T XP_011532175.1:p.Leu537=
XM_011533874.1:c.1609C>T XP_011532176.1:p.Leu537=
XM_011533875.1:c.1609C>T XP_011532177.1:p.Leu537=
XM_011533876.1:c.1609C>T XP_011532178.1:p.Leu537=
XM_011533877.1:c.820C>T XP_011532179.1:p.Leu274=
XM_011533878.1:c.1609C>T XP_011532180.1:p.Leu537=
XM_011533879.1:c.469C>T XP_011532181.1:p.Leu157=
XR_427279.2:n.2526C>T
NM_001322500.1:c.1609C>T NP_001309429.1:p.Leu537=
NM_001322501.1:c.703C>T NP_001309430.1:p.Leu235=
NM_017886.3:c.1609C>T NP_060356.2:p.Leu537=
NR_136342.1:n.2012C>T
NM_017886.4:c.1609C>T MANE Select NP_060356.2:p.Leu537=
NM_001322500.2:c.1609C>T NP_001309429.1:p.Leu537=
NM_001322501.2:c.703C>T NP_001309430.1:p.Leu235=
NR_136342.2:n.1675C>T