Canonical Allele Identifier: CA2695237993
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904101_154904102delinsTA , CM000685.2:g.154904101_154904102delinsTA GRCh38
NC_000023.10:g.154132376_154132377delinsTA , CM000685.1:g.154132376_154132377delinsTA GRCh37
NC_000023.9:g.153785570_153785571delinsTA NCBI36
NG_011403.1:g.123622_123623delinsTA
NG_011403.2:g.123622_123623delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5816-14_5816-13delinsTA MANE Select ENSP00000353393.4:n.5816-14_5816-13delins...
ENST00000360256.8:c.5816-14_5816-13delinsTA ENSP00000353393.4:n.5816-14_5816-13delins...
NM_000132.3:c.5816-14_5816-13delinsTA NP_000123.1:n.5816-14_5816-13delinsTA
XM_011531126.1:c.5711-14_5711-13delinsTA XP_011529428.1:n.5711-14_5711-13delinsTA
NM_000132.4:c.5816-14_5816-13delinsTA MANE Select NP_000123.1:n.5816-14_5816-13delinsTA