Canonical Allele Identifier: CA1360084023

Gene: ULK4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41883906C= , CM000665.2:g.41883906C=	GRCh38
NC_000003.11:g.41925398C= , CM000665.1:g.41925398C=	GRCh37
NC_000003.10:g.41900402C=	NCBI36
NG_051047.1:g.84115G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017886.4:c.1624G= MANE Select	NP_060356.2:p.Ala542=
ENST00000301831.9:c.1624G= MANE Select	ENSP00000301831.4:p.Ala542=
NM_001322500.1:c.1624G=	NP_001309429.1:p.Ala542=
NM_001322500.2:c.1624G=	NP_001309429.1:p.Ala542=
NM_001322501.1:c.718G=	NP_001309430.1:p.Ala240=
NM_001322501.2:c.718G=	NP_001309430.1:p.Ala240=
NM_017886.2:c.1624G=	NP_060356.2:p.Ala542=
NM_017886.3:c.1624G=	NP_060356.2:p.Ala542=
NR_136342.1:n.2027G=
NR_136342.2:n.1690G=
ENST00000301831.8:c.1624G=	ENSP00000301831.4:p.Ala542=
ENST00000420927.5:c.1624G=	ENSP00000412187.1:p.Ala542=
XM_005265261.3:c.1621G=	XP_005265318.1:p.Ala541=
XM_006713215.2:c.1267G=	XP_006713278.1:p.Ala423=
XM_011533872.1:c.1624G=	XP_011532174.1:p.Ala542=
XM_011533873.1:c.1624G=	XP_011532175.1:p.Ala542=
XM_011533874.1:c.1624G=	XP_011532176.1:p.Ala542=
XM_011533875.1:c.1624G=	XP_011532177.1:p.Ala542=
XM_011533876.1:c.1624G=	XP_011532178.1:p.Ala542=
XM_011533877.1:c.835G=	XP_011532179.1:p.Ala279=
XM_011533878.1:c.1624G=	XP_011532180.1:p.Ala542=
XM_011533879.1:c.484G=	XP_011532181.1:p.Ala162=
XR_427279.2:n.2541G=