Canonical Allele Identifier: CA352240443

Gene: ULK4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_017886.4:c.1624G>T MANE Select	NP_060356.2:p.Ala542Ser
ENST00000301831.9:c.1624G>T MANE Select	ENSP00000301831.4:p.Ala542Ser
NM_001322500.1:c.1624G>T	NP_001309429.1:p.Ala542Ser
NM_001322500.2:c.1624G>T	NP_001309429.1:p.Ala542Ser
NM_001322501.1:c.718G>T	NP_001309430.1:p.Ala240Ser
NM_001322501.2:c.718G>T	NP_001309430.1:p.Ala240Ser
NM_017886.2:c.1624G>T	NP_060356.2:p.Ala542Ser
NM_017886.3:c.1624G>T	NP_060356.2:p.Ala542Ser
NR_136342.1:n.2027G>T
NR_136342.2:n.1690G>T
ENST00000301831.8:c.1624G>T	ENSP00000301831.4:p.Ala542Ser
ENST00000420927.5:c.1624G>T	ENSP00000412187.1:p.Ala542Ser
XM_005265261.3:c.1621G>T	XP_005265318.1:p.Ala541Ser
XM_006713215.2:c.1267G>T	XP_006713278.1:p.Ala423Ser
XM_011533872.1:c.1624G>T	XP_011532174.1:p.Ala542Ser
XM_011533873.1:c.1624G>T	XP_011532175.1:p.Ala542Ser
XM_011533874.1:c.1624G>T	XP_011532176.1:p.Ala542Ser
XM_011533875.1:c.1624G>T	XP_011532177.1:p.Ala542Ser
XM_011533876.1:c.1624G>T	XP_011532178.1:p.Ala542Ser
XM_011533877.1:c.835G>T	XP_011532179.1:p.Ala279Ser
XM_011533878.1:c.1624G>T	XP_011532180.1:p.Ala542Ser
XM_011533879.1:c.484G>T	XP_011532181.1:p.Ala162Ser
XR_427279.2:n.2541G>T