Canonical Allele Identifier: CA433190815

Gene: ULK4

Linked Data

• MyVariant Identifiers: chr3:g.41925399T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883907T>C , CM000665.2:g.41883907T>C	GRCh38
NC_000003.11:g.41925399T>C , CM000665.1:g.41925399T>C	GRCh37
NC_000003.10:g.41900403T>C	NCBI36
NG_051047.1:g.84114A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301831.9:c.1623A>G MANE Select	ENSP00000301831.4:p.Thr541=
ENST00000301831.8:c.1623A>G	ENSP00000301831.4:p.Thr541=
ENST00000420927.5:c.1623A>G	ENSP00000412187.1:p.Thr541=
NM_017886.2:c.1623A>G	NP_060356.2:p.Thr541=
XM_005265261.3:c.1620A>G	XP_005265318.1:p.Thr540=
XM_006713215.2:c.1266A>G	XP_006713278.1:p.Thr422=
XM_011533872.1:c.1623A>G	XP_011532174.1:p.Thr541=
XM_011533873.1:c.1623A>G	XP_011532175.1:p.Thr541=
XM_011533874.1:c.1623A>G	XP_011532176.1:p.Thr541=
XM_011533875.1:c.1623A>G	XP_011532177.1:p.Thr541=
XM_011533876.1:c.1623A>G	XP_011532178.1:p.Thr541=
XM_011533877.1:c.834A>G	XP_011532179.1:p.Thr278=
XM_011533878.1:c.1623A>G	XP_011532180.1:p.Thr541=
XM_011533879.1:c.483A>G	XP_011532181.1:p.Thr161=
XR_427279.2:n.2540A>G
NM_001322500.1:c.1623A>G	NP_001309429.1:p.Thr541=
NM_001322501.1:c.717A>G	NP_001309430.1:p.Thr239=
NM_017886.3:c.1623A>G	NP_060356.2:p.Thr541=
NR_136342.1:n.2026A>G
NM_017886.4:c.1623A>G MANE Select	NP_060356.2:p.Thr541=
NM_001322500.2:c.1623A>G	NP_001309429.1:p.Thr541=
NM_001322501.2:c.717A>G	NP_001309430.1:p.Thr239=
NR_136342.2:n.1689A>G