Canonical Allele Identifier: CA907161587

Gene: ULK4

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41785534A>C , CM000665.2:g.41785534A>C	GRCh38
NC_000003.11:g.41827026A>C , CM000665.1:g.41827026A>C	GRCh37
NC_000003.10:g.41802030A>C	NCBI36
NG_051047.1:g.182487T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.2193+4127T>G MANE Select	ENSP00000301831.4:n.2193+4127T>G
ENST00000301831.8:c.2193+4127T>G	ENSP00000301831.4:n.2193+4127T>G
NM_017886.2:c.2193+4127T>G	NP_060356.2:n.2193+4127T>G
XM_005265261.3:c.2190+4127T>G	XP_005265318.1:n.2190+4127T>G
XM_006713215.2:c.1836+4127T>G	XP_006713278.1:n.1836+4127T>G
XM_011533872.1:c.2193+4127T>G	XP_011532174.1:n.2193+4127T>G
XM_011533873.1:c.2193+4127T>G	XP_011532175.1:n.2193+4127T>G
XM_011533874.1:c.2193+4127T>G	XP_011532176.1:n.2193+4127T>G
XM_011533875.1:c.2193+4127T>G	XP_011532177.1:n.2193+4127T>G
XM_011533876.1:c.2193+4127T>G	XP_011532178.1:n.2193+4127T>G
XM_011533877.1:c.1404+4127T>G	XP_011532179.1:n.1404+4127T>G
XM_011533878.1:c.2193+4127T>G	XP_011532180.1:n.2193+4127T>G
XM_011533879.1:c.1053+4127T>G	XP_011532181.1:n.1053+4127T>G
XM_011533880.1:c.366+4127T>G	XP_011532182.1:n.366+4127T>G
XR_427279.2:n.3110+4127T>G
NM_001322500.1:c.2193+4127T>G	NP_001309429.1:n.2193+4127T>G
NM_001322501.1:c.1287+4127T>G	NP_001309430.1:n.1287+4127T>G
NM_017886.3:c.2193+4127T>G	NP_060356.2:n.2193+4127T>G
NR_136342.1:n.2596+4127T>G
XM_011533880.3:c.366+4127T>G	XP_011532182.1:n.366+4127T>G
XM_024453612.1:c.324+4127T>G	XP_024309380.1:n.324+4127T>G
XM_024453613.1:c.366+4127T>G	XP_024309381.1:n.366+4127T>G
NM_017886.4:c.2193+4127T>G MANE Select	NP_060356.2:n.2193+4127T>G
NM_001322500.2:c.2193+4127T>G	NP_001309429.1:n.2193+4127T>G
NM_001322501.2:c.1287+4127T>G	NP_001309430.1:n.1287+4127T>G
NR_136342.2:n.2259+4127T>G