Canonical Allele Identifier: CA2830563605

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896269_154896270insGG , CM000685.2:g.154896269_154896270insGG	GRCh38
NC_000023.10:g.154124544_154124545insGG , CM000685.1:g.154124544_154124545insGG	GRCh37
NC_000023.9:g.153777738_153777739insGG	NCBI36
NG_011403.1:g.131454_131455insCC
NG_011403.2:g.131454_131455insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-38_6274-37insCC MANE Select	ENSP00000353393.4:n.6274-38_6274-37insCC
ENST00000360256.8:c.6274-38_6274-37insCC	ENSP00000353393.4:n.6274-38_6274-37insCC
NM_000132.3:c.6274-38_6274-37insCC	NP_000123.1:n.6274-38_6274-37insCC
XM_011531126.1:c.6169-38_6169-37insCC	XP_011529428.1:n.6169-38_6169-37insCC
NM_000132.4:c.6274-38_6274-37insCC MANE Select	NP_000123.1:n.6274-38_6274-37insCC