Canonical Allele Identifier: CA16141281

Gene: ULK4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41946428T>C , CM000665.2:g.41946428T>C	GRCh38
NC_000003.11:g.41987920T>C , CM000665.1:g.41987920T>C	GRCh37
NC_000003.10:g.41962924T>C	NCBI36
NG_051047.1:g.21593A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301831.9:c.138+8194A>G MANE Select	ENSP00000301831.4:n.138+8194A>G
ENST00000301831.8:c.138+8194A>G	ENSP00000301831.4:n.138+8194A>G
ENST00000414606.1:c.138+8194A>G	ENSP00000399382.1:n.138+8194A>G
ENST00000420927.5:c.138+8194A>G	ENSP00000412187.1:n.138+8194A>G
ENST00000431379.5:c.138+8194A>G	ENSP00000391849.1:n.138+8194A>G
ENST00000453224.5:c.138+8194A>G	ENSP00000401414.1:n.138+8194A>G
ENST00000459802.5:n.63-8231A>G
ENST00000460978.1:n.226+8194A>G
ENST00000497684.1:n.177+8194A>G
NM_017886.2:c.138+8194A>G	NP_060356.2:n.138+8194A>G
XM_005265261.3:c.138+8194A>G	XP_005265318.1:n.138+8194A>G
XM_006713215.2:c.-130+8194A>G	XP_006713278.1:n.-130+8194A>G
XM_011533872.1:c.138+8194A>G	XP_011532174.1:n.138+8194A>G
XM_011533873.1:c.138+8194A>G	XP_011532175.1:n.138+8194A>G
XM_011533874.1:c.138+8194A>G	XP_011532176.1:n.138+8194A>G
XM_011533875.1:c.138+8194A>G	XP_011532177.1:n.138+8194A>G
XM_011533876.1:c.138+8194A>G	XP_011532178.1:n.138+8194A>G
XM_011533878.1:c.138+8194A>G	XP_011532180.1:n.138+8194A>G
XR_427279.2:n.1055+8194A>G
NM_001322500.1:c.138+8194A>G	NP_001309429.1:n.138+8194A>G
NM_001322501.1:c.-693+8194A>G	NP_001309430.1:n.-693+8194A>G
NM_017886.3:c.138+8194A>G	NP_060356.2:n.138+8194A>G
NR_136342.1:n.611+8194A>G
NM_017886.4:c.138+8194A>G MANE Select	NP_060356.2:n.138+8194A>G
NM_001322500.2:c.138+8194A>G	NP_001309429.1:n.138+8194A>G
NM_001322501.2:c.-693+8194A>G	NP_001309430.1:n.-693+8194A>G
NR_136342.2:n.274+8194A>G