Canonical Allele Identifier: CA1624564274

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43524804_43524816delinsTCCTTCCCCCATG , CM000668.2:g.43524804_43524816delinsTCCTTCCCCCATG GRCh38
NC_000006.11:g.43492542_43492554delinsTCCTTCCCCCATG , CM000668.1:g.43492542_43492554delinsTCCTTCCCCCATG GRCh37
NC_000006.10:g.43600520_43600532delinsTCCTTCCCCCATG NCBI36
NG_028283.3:g.20103_20115delinsTCCTTCCCCCATG
NG_051658.1:g.56260_56272delinsCATGGGGGAAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.3312+15_3312+27delinsCATGGGGGAAGGA (XPO5) MANE Select ENSP00000265351.7:n.3312+15_3312+27delinsCATGGGGGAAGGA
ENST00000607635.2:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) ENSP00000496683.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
ENST00000643341.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) ENSP00000496018.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
ENST00000643799.1:c.*17+3487_*17+3499delinsTCCTTCCCCCATG (POLR1C) ENSP00000494529.1:n.*17+3487_*17+3499delinsTCCTTCCCCCATG
ENST00000646433.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) ENSP00000494368.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
ENST00000646700.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) ENSP00000495521.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
ENST00000265351.11:c.3312+15_3312+27delinsCATGGGGGAAGGA (XPO5) ENSP00000265351.7:n.3312+15_3312+27delinsCATGGGGGAAGGA
ENST00000304004.7:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) ENSP00000307212.3:n.922+3756_922+3768delinsTCCTTCCCCCATG
ENST00000455285.2:c.656+15_656+27delinsCATGGGGGAAGGA (XPO5)
ENST00000455854.2:n.1795+15_1795+27delinsCATGGGGGAAGGA (XPO5)
ENST00000486936.2:c.499+15_499+27delinsCATGGGGGAAGGA (XPO5)
ENST00000488195.6:n.709+15_709+27delinsCATGGGGGAAGGA (XPO5)
NM_020750.2:c.3312+15_3312+27delinsCATGGGGGAAGGA (XPO5) NP_065801.1:n.3312+15_3312+27delinsCATGGGGGAAGGA
XM_005249491.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) XP_005249548.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
XM_011515000.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) XP_011513302.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
NM_001318876.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) NP_001305805.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
NM_001363658.1:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) NP_001350587.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
NR_144392.1:n.3661+15_3661+27delinsCATGGGGGAAGGA (XPO5)
NM_020750.3:c.3312+15_3312+27delinsCATGGGGGAAGGA (XPO5) MANE Select NP_065801.1:n.3312+15_3312+27delinsCATGGGGGAAGGA
NM_001363658.2:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) NP_001350587.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
NM_001318876.2:c.922+3756_922+3768delinsTCCTTCCCCCATG (POLR1C) NP_001305805.1:n.922+3756_922+3768delinsTCCTTCCCCCATG
NR_144392.2:n.3624+15_3624+27delinsCATGGGGGAAGGA (XPO5)