Canonical Allele Identifier: CA3825788

Linked Data

dbSNP Id: rs776638949

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43524423_43524424del , CM000668.2:g.43524423_43524424del GRCh38
NC_000006.11:g.43492161_43492162del , CM000668.1:g.43492161_43492162del GRCh37
NC_000006.10:g.43600139_43600140del NCBI36
NG_028283.3:g.19722_19723del
NG_051658.1:g.56652_56653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.3477+47_3477+48del (XPO5) MANE Select ENSP00000265351.7:n.3477+47_3477+48del
ENST00000607635.2:c.922+3375_922+3376del (POLR1C) ENSP00000496683.1:n.922+3375_922+3376del
ENST00000643341.1:c.922+3375_922+3376del (POLR1C) ENSP00000496018.1:n.922+3375_922+3376del
ENST00000643799.1:c.*17+3106_*17+3107del (POLR1C) ENSP00000494529.1:n.*17+3106_*17+3107del
ENST00000646433.1:c.922+3375_922+3376del (POLR1C) ENSP00000494368.1:n.922+3375_922+3376del
ENST00000646700.1:c.922+3375_922+3376del (POLR1C) ENSP00000495521.1:n.922+3375_922+3376del
ENST00000265351.11:c.3477+47_3477+48del (XPO5) ENSP00000265351.7:n.3477+47_3477+48del
ENST00000304004.7:c.922+3375_922+3376del (POLR1C) ENSP00000307212.3:n.922+3375_922+3376del
ENST00000455854.2:n.1960+47_1960+48del (XPO5)
NM_020750.2:c.3477+47_3477+48del (XPO5) NP_065801.1:n.3477+47_3477+48del
XM_005249491.1:c.922+3375_922+3376del (POLR1C) XP_005249548.1:n.922+3375_922+3376del
XM_011515000.1:c.922+3375_922+3376del (POLR1C) XP_011513302.1:n.922+3375_922+3376del
NM_001318876.1:c.922+3375_922+3376del (POLR1C) NP_001305805.1:n.922+3375_922+3376del
NM_001363658.1:c.922+3375_922+3376del (POLR1C) NP_001350587.1:n.922+3375_922+3376del
NR_144392.1:n.3826+47_3826+48del (XPO5)
NM_020750.3:c.3477+47_3477+48del (XPO5) MANE Select NP_065801.1:n.3477+47_3477+48del
NM_001363658.2:c.922+3375_922+3376del (POLR1C) NP_001350587.1:n.922+3375_922+3376del
NM_001318876.2:c.922+3375_922+3376del (POLR1C) NP_001305805.1:n.922+3375_922+3376del
NR_144392.2:n.3789+47_3789+48del (XPO5)