Canonical Allele Identifier: CA11471769
Gene: ULK4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41950916G>A , CM000665.2:g.41950916G>A GRCh38
NC_000003.11:g.41992408G>A , CM000665.1:g.41992408G>A GRCh37
NC_000003.10:g.41967412G>A NCBI36
NG_051047.1:g.17105C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301831.9:c.138+3706C>T MANE Select ENSP00000301831.4:n.138+3706C>T
ENST00000301831.8:c.138+3706C>T ENSP00000301831.4:n.138+3706C>T
ENST00000414606.1:c.138+3706C>T ENSP00000399382.1:n.138+3706C>T
ENST00000420927.5:c.138+3706C>T ENSP00000412187.1:n.138+3706C>T
ENST00000431379.5:c.138+3706C>T ENSP00000391849.1:n.138+3706C>T
ENST00000453224.5:c.138+3706C>T ENSP00000401414.1:n.138+3706C>T
ENST00000459802.5:n.62+11100C>T
ENST00000460978.1:n.226+3706C>T
ENST00000497684.1:n.177+3706C>T
NM_017886.2:c.138+3706C>T NP_060356.2:n.138+3706C>T
XM_005265261.3:c.138+3706C>T XP_005265318.1:n.138+3706C>T
XM_006713215.2:c.-130+3706C>T XP_006713278.1:n.-130+3706C>T
XM_011533872.1:c.138+3706C>T XP_011532174.1:n.138+3706C>T
XM_011533873.1:c.138+3706C>T XP_011532175.1:n.138+3706C>T
XM_011533874.1:c.138+3706C>T XP_011532176.1:n.138+3706C>T
XM_011533875.1:c.138+3706C>T XP_011532177.1:n.138+3706C>T
XM_011533876.1:c.138+3706C>T XP_011532178.1:n.138+3706C>T
XM_011533878.1:c.138+3706C>T XP_011532180.1:n.138+3706C>T
XR_427279.2:n.1055+3706C>T
NM_001322500.1:c.138+3706C>T NP_001309429.1:n.138+3706C>T
NM_001322501.1:c.-693+3706C>T NP_001309430.1:n.-693+3706C>T
NM_017886.3:c.138+3706C>T NP_060356.2:n.138+3706C>T
NR_136342.1:n.611+3706C>T
NM_017886.4:c.138+3706C>T MANE Select NP_060356.2:n.138+3706C>T
NM_001322500.2:c.138+3706C>T NP_001309429.1:n.138+3706C>T
NM_001322501.2:c.-693+3706C>T NP_001309430.1:n.-693+3706C>T
NR_136342.2:n.274+3706C>T
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