Canonical Allele Identifier: CA2623807023

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113129704_113129705insCCCC , CM000675.2:g.113129704_113129705insCCCC GRCh38
NC_000013.10:g.113784018_113784019insCCCC , CM000675.1:g.113784018_113784019insCCCC GRCh37
NC_000013.9:g.112832019_112832020insCCCC NCBI36
NG_009258.1:g.11906_11907insCCCC , LRG_548:g.11906_11907insCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.231+92_231+93insCCCC (F10) MANE Select ENSP00000364709.3:n.231+92_231+93insCCCC
ENST00000375551.7:c.231+92_231+93insCCCC (F10) ENSP00000364701.3:n.231+92_231+93insCCCC
ENST00000375559.7:c.231+92_231+93insCCCC (F10) ENSP00000364709.3:n.231+92_231+93insCCCC
ENST00000409306.5:c.231+92_231+93insCCCC (F10) ENSP00000387092.1:n.231+92_231+93insCCCC
ENST00000410083.6:c.231+92_231+93insCCCC (F10) ENSP00000386320.2:n.231+92_231+93insCCCC
ENST00000477269.5:n.268+92_268+93insCCCC (F10)
ENST00000483537.1:n.251+92_251+93insCCCC (F10)
NM_000504.3:c.231+92_231+93insCCCC , LRG_548t1:c.231+92_231+93insCCCC (F10) NP_000495.1:n.231+92_231+93insCCCC
NM_001312674.1:c.231+92_231+93insCCCC (F10) NP_001299603.1:n.231+92_231+93insCCCC
NM_001312675.1:c.231+92_231+93insCCCC (F10) NP_001299604.1:n.231+92_231+93insCCCC
NR_126424.1:n.41+303_41+304insGGGG (F10-AS1)
NM_000504.4:c.231+92_231+93insCCCC (F10) MANE Select NP_000495.1:n.231+92_231+93insCCCC
NM_001312674.2:c.231+92_231+93insCCCC (F10) NP_001299603.1:n.231+92_231+93insCCCC
NM_001312675.2:c.231+92_231+93insCCCC (F10) NP_001299604.1:n.231+92_231+93insCCCC