Canonical Allele Identifier: CA2466835687
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928436_154928440delinsTTCTC , CM000685.2:g.154928436_154928440delinsTTCTC GRCh38
NC_000023.10:g.154156711_154156715delinsTTCTC , CM000685.1:g.154156711_154156715delinsTTCTC GRCh37
NC_000023.9:g.153809905_153809909delinsTTCTC NCBI36
NG_011403.1:g.99284_99288delinsGAGAA
NG_011403.2:g.99284_99288delinsGAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5219+131_5219+135delinsGAGAA MANE Select ENSP00000353393.4:n.5219+131_5219+135delinsGAGAA
ENST00000360256.8:c.5219+131_5219+135delinsGAGAA ENSP00000353393.4:n.5219+131_5219+135delinsGAGAA
NM_000132.3:c.5219+131_5219+135delinsGAGAA NP_000123.1:n.5219+131_5219+135delinsGAGAA
XM_011531126.1:c.5114+131_5114+135delinsGAGAA XP_011529428.1:n.5114+131_5114+135delinsGAGAA
NM_000132.4:c.5219+131_5219+135delinsGAGAA MANE Select NP_000123.1:n.5219+131_5219+135delinsGAGAA
Search 100 bp 5'
Search 100 bp 3'