Canonical Allele Identifier: CA917735916

Linked Data

dbSNP Id: rs369159546

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43524824_43524825insCCCTTCCCCCATGCCTTCCCC , CM000668.2:g.43524824_43524825insCCCTTCCCCCATGCCTTCCCC GRCh38
NC_000006.11:g.43492562_43492563insCCCTTCCCCCATGCCTTCCCC , CM000668.1:g.43492562_43492563insCCCTTCCCCCATGCCTTCCCC GRCh37
NC_000006.10:g.43600540_43600541insCCCTTCCCCCATGCCTTCCCC NCBI36
NG_028283.3:g.20123_20124insCCCTTCCCCCATGCCTTCCCC
NG_051658.1:g.56271_56272insGGGGGAAGGCATGGGGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG (XPO5) MANE Select ENSP00000265351.7:n.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG
ENST00000607635.2:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000496683.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC...
ENST00000643341.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000496018.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC...
ENST00000643799.1:c.*17+3507_*17+3508insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000494529.1:n.*17+3507_*17+3508insCCCTTCCCCCATGCCTTCCCC...
ENST00000646433.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000494368.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC...
ENST00000646700.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000495521.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC...
ENST00000265351.11:c.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG (XPO5) ENSP00000265351.7:n.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG
ENST00000304004.7:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) ENSP00000307212.3:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC...
ENST00000455285.2:c.656+26_656+27insGGGGGAAGGCATGGGGGAAGG (XPO5)
ENST00000455854.2:n.1795+26_1795+27insGGGGGAAGGCATGGGGGAAGG (XPO5)
ENST00000486936.2:c.499+26_499+27insGGGGGAAGGCATGGGGGAAGG (XPO5)
ENST00000488195.6:n.709+26_709+27insGGGGGAAGGCATGGGGGAAGG (XPO5)
NM_020750.2:c.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG (XPO5) NP_065801.1:n.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG
XM_005249491.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) XP_005249548.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
XM_011515000.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) XP_011513302.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
NM_001318876.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) NP_001305805.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
NM_001363658.1:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) NP_001350587.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
NR_144392.1:n.3661+26_3661+27insGGGGGAAGGCATGGGGGAAGG (XPO5)
NM_020750.3:c.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG (XPO5) MANE Select NP_065801.1:n.3312+26_3312+27insGGGGGAAGGCATGGGGGAAGG
NM_001363658.2:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) NP_001350587.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
NM_001318876.2:c.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC (POLR1C) NP_001305805.1:n.922+3776_922+3777insCCCTTCCCCCATGCCTTCCCC
NR_144392.2:n.3624+26_3624+27insGGGGGAAGGCATGGGGGAAGG (XPO5)