Canonical Allele Identifier: CA2623810349
Gene: F10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149399_113149400insCGAACACCGA , CM000675.2:g.113149399_113149400insCGAACACCGA GRCh38
NC_000013.10:g.113803713_113803714insCGAACACCGA , CM000675.1:g.113803713_113803714insCGAACACCGA GRCh37
NC_000013.9:g.112851714_112851715insCGAACACCGA NCBI36
NG_009258.1:g.31601_31602insCGAACACCGA , LRG_548:g.31601_31602insCGAACACCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1349_1350insCGAACACCGA MANE Select ENSP00000364709.3:p.Ile451GlufsTer?
ENST00000375551.7:c.*340_*341insCGAACACCGA ENSP00000364701.3:n.*340_*341insCGAACACCGA
ENST00000375559.7:c.1349_1350insCGAACACCGA ENSP00000364709.3:p.Ile451GlufsTer?
ENST00000409306.5:c.*340_*341insCGAACACCGA ENSP00000387092.1:n.*340_*341insCGAACACCGA
NM_000504.3:c.1349_1350insCGAACACCGA , LRG_548t1:c.1349_1350insCGAACACCGA NP_000495.1:p.Ile451GlufsTer?
NM_001312674.1:c.1217_1218insCGAACACCGA NP_001299603.1:p.Ile407GlufsTer?
NM_001312675.1:c.*340_*341insCGAACACCGA NP_001299604.1:n.*340_*341insCGAACACCGA
NM_000504.4:c.1349_1350insCGAACACCGA MANE Select NP_000495.1:p.Ile451GlufsTer?
NM_001312674.2:c.1217_1218insCGAACACCGA NP_001299603.1:p.Ile407GlufsTer?
NM_001312675.2:c.*340_*341insCGAACACCGA NP_001299604.1:n.*340_*341insCGAACACCGA