Canonical Allele Identifier: CA353840644
Community Standard Title: NM_020654.5(SENP7):c.1474C>T (p.Gln492Ter)
Gene: SENP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101364836G>A , CM000665.2:g.101364836G>A GRCh38
NC_000003.11:g.101083680G>A , CM000665.1:g.101083680G>A GRCh37
NC_000003.10:g.102566370G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020654.5:c.1474C>T MANE Select NP_065705.3:p.Gln492Ter
ENST00000394095.7:c.1474C>T MANE Select ENSP00000377655.2:p.Gln492Ter
NM_001077203.2:c.1279C>T NP_001070671.1:p.Gln427Ter
NM_001077203.3:c.1279C>T NP_001070671.1:p.Gln427Ter
NM_001282801.1:c.1276C>T NP_001269730.1:p.Gln426Ter
NM_001282801.2:c.1276C>T NP_001269730.1:p.Gln426Ter
NM_001282802.1:c.1375C>T NP_001269731.1:p.Gln459Ter
NM_001282802.2:c.1375C>T NP_001269731.1:p.Gln459Ter
NM_001282803.1:c.982C>T NP_001269732.1:p.Gln328Ter
NM_001282803.2:c.982C>T NP_001269732.1:p.Gln328Ter
NM_020654.4:c.1474C>T NP_065705.3:p.Gln492Ter
ENST00000314261.11:c.1276C>T ENSP00000313624.7:p.Gln426Ter
ENST00000348610.3:c.1375C>T ENSP00000342159.3:p.Gln459Ter
ENST00000394091.5:c.982C>T ENSP00000377651.1:p.Gln328Ter
ENST00000394094.6:c.1279C>T ENSP00000377654.2:p.Gln427Ter
ENST00000394095.6:c.1474C>T ENSP00000377655.2:p.Gln492Ter
XM_005247662.3:c.1081C>T XP_005247719.1:p.Gln361Ter
XM_005247662.5:c.1081C>T XP_005247719.1:p.Gln361Ter
XM_011513038.1:c.1477C>T XP_011511340.1:p.Gln493Ter
XM_011513038.3:c.1477C>T XP_011511340.1:p.Gln493Ter
XM_011513039.1:c.1378C>T XP_011511341.1:p.Gln460Ter
XM_011513039.3:c.1378C>T XP_011511341.1:p.Gln460Ter
XM_011513040.1:c.1282C>T XP_011511342.1:p.Gln428Ter
XM_011513040.3:c.1282C>T XP_011511342.1:p.Gln428Ter
XM_011513041.1:c.1279C>T XP_011511343.1:p.Gln427Ter
XM_011513041.3:c.1279C>T XP_011511343.1:p.Gln427Ter
XM_011513042.1:c.1084C>T XP_011511344.1:p.Gln362Ter
XM_011513042.3:c.1084C>T XP_011511344.1:p.Gln362Ter
XM_011513043.1:c.1477C>T XP_011511345.1:p.Gln493Ter
XM_011513044.1:c.1477C>T XP_011511346.1:p.Gln493Ter
XM_011513045.1:c.1477C>T XP_011511347.1:p.Gln493Ter
XM_011513045.3:c.1477C>T XP_011511347.1:p.Gln493Ter
XM_017006924.1:c.1378C>T XP_016862413.1:p.Gln460Ter
XM_017006925.1:c.1375C>T XP_016862414.1:p.Gln459Ter
XM_017006926.1:c.1180C>T XP_016862415.1:p.Gln394Ter
XM_017006927.1:c.1177C>T XP_016862416.1:p.Gln393Ter
XM_017006928.2:c.1477C>T XP_016862417.1:p.Gln493Ter
XR_001740218.2:n.2230C>T