Canonical Allele Identifier: CA2466828227

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904190_154904192delinsGAT , CM000685.2:g.154904190_154904192delinsGAT	GRCh38
NC_000023.10:g.154132465_154132467delinsGAT , CM000685.1:g.154132465_154132467delinsGAT	GRCh37
NC_000023.9:g.153785659_153785661delinsGAT	NCBI36
NG_011403.1:g.123532_123534delinsATC
NG_011403.2:g.123532_123534delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-104_5816-102delinsATC MANE Select	ENSP00000353393.4:n.5816-104_5816-102delinsATC
ENST00000360256.8:c.5816-104_5816-102delinsATC	ENSP00000353393.4:n.5816-104_5816-102delinsATC
NM_000132.3:c.5816-104_5816-102delinsATC	NP_000123.1:n.5816-104_5816-102delinsATC
XM_011531126.1:c.5711-104_5711-102delinsATC	XP_011529428.1:n.5711-104_5711-102delinsATC
NM_000132.4:c.5816-104_5816-102delinsATC MANE Select	NP_000123.1:n.5816-104_5816-102delinsATC