Canonical Allele Identifier: CA35569184
Community Standard Title: NM_006618.5(KDM5B):c.3841C>T (p.Arg1281Ter)
Gene: KDM5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202733469G>A , CM000663.2:g.202733469G>A GRCh38
NC_000001.10:g.202702597G>A , CM000663.1:g.202702597G>A GRCh37
NC_000001.9:g.200969220G>A NCBI36
NG_050659.1:g.80939C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006618.5:c.3841C>T MANE Select NP_006609.3:p.Arg1281Ter
ENST00000367265.9:c.3841C>T MANE Select ENSP00000356234.3:p.Arg1281Ter
NM_001314042.1:c.3949C>T NP_001300971.1:p.Arg1317Ter
NM_001314042.2:c.3949C>T NP_001300971.1:p.Arg1317Ter
NM_001347591.1:c.3706C>T NP_001334520.1:p.Arg1236Ter
NM_001347591.2:c.3706C>T NP_001334520.1:p.Arg1236Ter
NM_001399817.1:c.3826C>T NP_001386746.1:p.Arg1276Ter
NM_006618.3:c.3841C>T NP_006609.3:p.Arg1281Ter
NM_006618.4:c.3841C>T NP_006609.3:p.Arg1281Ter
ENST00000235790.8:c.3367C>T ENSP00000235790.4:p.Arg1123Ter
ENST00000235790.9:c.3367C>T ENSP00000235790.4:p.Arg1123Ter
ENST00000367264.6:c.3949C>T ENSP00000356233.2:p.Arg1317Ter
ENST00000367264.7:c.3949C>T ENSP00000356233.2:p.Arg1317Ter
ENST00000367265.7:c.3841C>T ENSP00000356234.3:p.Arg1281Ter
ENST00000472822.5:n.601C>T
ENST00000472822.6:n.847C>T
ENST00000498276.2:n.1927C>T
ENST00000647657.1:n.804C>T
ENST00000647757.1:n.3727C>T
ENST00000648056.1:c.3826C>T ENSP00000497113.1:p.Arg1276Ter
ENST00000648338.1:c.3841C>T ENSP00000497564.1:p.Arg1281Ter
ENST00000648469.1:c.3718C>T ENSP00000497827.1:p.Arg1240Ter
ENST00000648473.1:c.3841C>T ENSP00000497743.1:p.Arg1281Ter
ENST00000649089.1:c.1885C>T
ENST00000649230.1:n.3067C>T
ENST00000649400.1:n.1573C>T
ENST00000649542.1:n.3724C>T
ENST00000649770.1:c.3718C>T ENSP00000497288.1:p.Arg1240Ter
ENST00000650417.1:c.*3267C>T ENSP00000497297.1:n.*3267C>T
ENST00000650506.1:n.2017C>T
ENST00000650569.1:c.3706C>T ENSP00000497671.1:p.Arg1236Ter
XM_011509087.1:c.3949C>T XP_011507389.1:p.Arg1317Ter
XM_011509088.1:c.3706C>T XP_011507390.1:p.Arg1236Ter
XM_011509089.1:c.3868C>T XP_011507391.1:p.Arg1290Ter
XM_011509090.1:c.3475C>T XP_011507392.1:p.Arg1159Ter
XM_011509090.3:c.3475C>T XP_011507392.1:p.Arg1159Ter
XM_011509091.1:c.3475C>T XP_011507393.1:p.Arg1159Ter
XM_011509091.2:c.3475C>T XP_011507393.1:p.Arg1159Ter
XM_011509092.1:c.3367C>T XP_011507394.1:p.Arg1123Ter
XM_011509092.2:c.3367C>T XP_011507394.1:p.Arg1123Ter