Canonical Allele Identifier: CA2120153837

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113129541_113129543delinsGAA , CM000675.2:g.113129541_113129543delinsGAA GRCh38
NC_000013.10:g.113783855_113783857delinsGAA , CM000675.1:g.113783855_113783857delinsGAA GRCh37
NC_000013.9:g.112831856_112831858delinsGAA NCBI36
NG_009258.1:g.11743_11745delinsGAA , LRG_548:g.11743_11745delinsGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000375559.8:c.160_162delinsGAA (F10) MANE Select ENSP00000364709.3:p.Glu54=
ENST00000375551.7:c.160_162delinsGAA (F10) ENSP00000364701.3:p.Glu54=
ENST00000375559.7:c.160_162delinsGAA (F10) ENSP00000364709.3:p.Glu54=
ENST00000409306.5:c.160_162delinsGAA (F10) ENSP00000387092.1:p.Glu54=
ENST00000410083.6:c.160_162delinsGAA (F10) ENSP00000386320.2:p.Glu54=
ENST00000477269.5:n.197_199delinsGAA (F10)
ENST00000483537.1:n.180_182delinsGAA (F10)
NM_000504.3:c.160_162delinsGAA , LRG_548t1:c.160_162delinsGAA (F10) NP_000495.1:p.Glu54=
NM_001312674.1:c.160_162delinsGAA (F10) NP_001299603.1:p.Glu54=
NM_001312675.1:c.160_162delinsGAA (F10) NP_001299604.1:p.Glu54=
NR_126424.1:n.41+463_41+465delinsTTC (F10-AS1)
NM_000504.4:c.160_162delinsGAA (F10) MANE Select NP_000495.1:p.Glu54=
NM_001312674.2:c.160_162delinsGAA (F10) NP_001299603.1:p.Glu54=
NM_001312675.2:c.160_162delinsGAA (F10) NP_001299604.1:p.Glu54=