Canonical Allele Identifier: CA2770835562

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43524429_43524432del , CM000668.2:g.43524429_43524432del GRCh38
NC_000006.11:g.43492167_43492170del , CM000668.1:g.43492167_43492170del GRCh37
NC_000006.10:g.43600145_43600148del NCBI36
NG_028283.3:g.19728_19731del
NG_051658.1:g.56644_56647del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.3477+39_3477+42del (XPO5) MANE Select ENSP00000265351.7:n.3477+39_3477+42del
ENST00000607635.2:c.922+3381_922+3384del (POLR1C) ENSP00000496683.1:n.922+3381_922+3384del
ENST00000643341.1:c.922+3381_922+3384del (POLR1C) ENSP00000496018.1:n.922+3381_922+3384del
ENST00000643799.1:c.*17+3112_*17+3115del (POLR1C) ENSP00000494529.1:n.*17+3112_*17+3115del
ENST00000646433.1:c.922+3381_922+3384del (POLR1C) ENSP00000494368.1:n.922+3381_922+3384del
ENST00000646700.1:c.922+3381_922+3384del (POLR1C) ENSP00000495521.1:n.922+3381_922+3384del
ENST00000265351.11:c.3477+39_3477+42del (XPO5) ENSP00000265351.7:n.3477+39_3477+42del
ENST00000304004.7:c.922+3381_922+3384del (POLR1C) ENSP00000307212.3:n.922+3381_922+3384del
ENST00000455854.2:n.1960+39_1960+42del (XPO5)
NM_020750.2:c.3477+39_3477+42del (XPO5) NP_065801.1:n.3477+39_3477+42del
XM_005249491.1:c.922+3381_922+3384del (POLR1C) XP_005249548.1:n.922+3381_922+3384del
XM_011515000.1:c.922+3381_922+3384del (POLR1C) XP_011513302.1:n.922+3381_922+3384del
NM_001318876.1:c.922+3381_922+3384del (POLR1C) NP_001305805.1:n.922+3381_922+3384del
NM_001363658.1:c.922+3381_922+3384del (POLR1C) NP_001350587.1:n.922+3381_922+3384del
NR_144392.1:n.3826+39_3826+42del (XPO5)
NM_020750.3:c.3477+39_3477+42del (XPO5) MANE Select NP_065801.1:n.3477+39_3477+42del
NM_001363658.2:c.922+3381_922+3384del (POLR1C) NP_001350587.1:n.922+3381_922+3384del
NM_001318876.2:c.922+3381_922+3384del (POLR1C) NP_001305805.1:n.922+3381_922+3384del
NR_144392.2:n.3789+39_3789+42del (XPO5)