Canonical Allele Identifier: CA2838273887
Gene: HOOK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59815228A>T , CM000663.2:g.59815228A>T GRCh38
NC_000001.10:g.60280900A>T , CM000663.1:g.60280900A>T GRCh37
NC_000001.9:g.60053488A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685567.1:c.-187A>T ENSP00000509959.1:n.-187A>T
ENST00000686522.1:c.63+48A>T ENSP00000509232.1:n.63+48A>T
ENST00000686716.1:n.166+48A>T
ENST00000687049.1:c.-107+48A>T ENSP00000509189.1:n.-107+48A>T
ENST00000371208.5:c.63+48A>T MANE Select ENSP00000360252.3:n.63+48A>T
ENST00000371208.3:c.63+48A>T ENSP00000360252.3:n.63+48A>T
ENST00000455990.5:c.63+48A>T ENSP00000398860.1:n.63+48A>T
ENST00000465876.5:n.57A>T
NM_015888.4:c.63+48A>T NP_056972.1:n.63+48A>T
XM_006710676.1:c.63+48A>T XP_006710739.1:n.63+48A>T
XM_011541562.1:c.-211+48A>T XP_011539864.1:n.-211+48A>T
XM_011541563.1:c.63+48A>T XP_011539865.1:n.63+48A>T
XR_246271.1:n.259+48A>T
XR_946665.1:n.259+48A>T
XR_947427.1:n.103+410T>A
XM_011541562.2:c.-211+48A>T XP_011539864.1:n.-211+48A>T
XM_017001424.1:c.63+48A>T XP_016856913.1:n.63+48A>T
NM_015888.5:c.63+48A>T NP_056972.1:n.63+48A>T
NM_015888.6:c.63+48A>T MANE Select NP_056972.1:n.63+48A>T