Canonical Allele Identifier: CA433190822

Gene: ULK4

Linked Data

• MyVariant Identifiers: chr3:g.41925411C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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