Canonical Allele Identifier: CA2695152099

Gene: F8

Linked Data

• gnomAD v4: X-154896324-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896324_154896325insA , CM000685.2:g.154896324_154896325insA	GRCh38
NC_000023.10:g.154124599_154124600insA , CM000685.1:g.154124599_154124600insA	GRCh37
NC_000023.9:g.153777793_153777794insA	NCBI36
NG_011403.1:g.131399_131400insT
NG_011403.2:g.131399_131400insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-93_6274-92insT MANE Select	ENSP00000353393.4:n.6274-93_6274-92insT
ENST00000360256.8:c.6274-93_6274-92insT	ENSP00000353393.4:n.6274-93_6274-92insT
NM_000132.3:c.6274-93_6274-92insT	NP_000123.1:n.6274-93_6274-92insT
XM_011531126.1:c.6169-93_6169-92insT	XP_011529428.1:n.6169-93_6169-92insT
NM_000132.4:c.6274-93_6274-92insT MANE Select	NP_000123.1:n.6274-93_6274-92insT