Canonical Allele Identifier: CA567152758

Linked Data

dbSNP Id: rs1193871224

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43524813dup , CM000668.2:g.43524813dup GRCh38
NC_000006.11:g.43492551dup , CM000668.1:g.43492551dup GRCh37
NC_000006.10:g.43600529dup NCBI36
NG_028283.3:g.20112dup
NG_051658.1:g.56267dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.3312+22dup (XPO5) MANE Select ENSP00000265351.7:n.3312+22dup
ENST00000607635.2:c.922+3765dup (POLR1C) ENSP00000496683.1:n.922+3765dup
ENST00000643341.1:c.922+3765dup (POLR1C) ENSP00000496018.1:n.922+3765dup
ENST00000643799.1:c.*17+3496dup (POLR1C) ENSP00000494529.1:n.*17+3496dup
ENST00000646433.1:c.922+3765dup (POLR1C) ENSP00000494368.1:n.922+3765dup
ENST00000646700.1:c.922+3765dup (POLR1C) ENSP00000495521.1:n.922+3765dup
ENST00000265351.11:c.3312+22dup (XPO5) ENSP00000265351.7:n.3312+22dup
ENST00000304004.7:c.922+3765dup (POLR1C) ENSP00000307212.3:n.922+3765dup
ENST00000455285.2:c.656+22dup (XPO5)
ENST00000455854.2:n.1795+22dup (XPO5)
ENST00000486936.2:c.499+22dup (XPO5)
ENST00000488195.6:n.709+22dup (XPO5)
NM_020750.2:c.3312+22dup (XPO5) NP_065801.1:n.3312+22dup
XM_005249491.1:c.922+3765dup (POLR1C) XP_005249548.1:n.922+3765dup
XM_011515000.1:c.922+3765dup (POLR1C) XP_011513302.1:n.922+3765dup
NM_001318876.1:c.922+3765dup (POLR1C) NP_001305805.1:n.922+3765dup
NM_001363658.1:c.922+3765dup (POLR1C) NP_001350587.1:n.922+3765dup
NR_144392.1:n.3661+22dup (XPO5)
NM_020750.3:c.3312+22dup (XPO5) MANE Select NP_065801.1:n.3312+22dup
NM_001363658.2:c.922+3765dup (POLR1C) NP_001350587.1:n.922+3765dup
NM_001318876.2:c.922+3765dup (POLR1C) NP_001305805.1:n.922+3765dup
NR_144392.2:n.3624+22dup (XPO5)