Canonical Allele Identifier: CA2695152117

Gene: F8

Linked Data

• gnomAD v4: X-154896343-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896344_154896345del , CM000685.2:g.154896344_154896345del	GRCh38
NC_000023.10:g.154124619_154124620del , CM000685.1:g.154124619_154124620del	GRCh37
NC_000023.9:g.153777813_153777814del	NCBI36
NG_011403.1:g.131379_131380del
NG_011403.2:g.131379_131380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-113_6274-112del MANE Select	ENSP00000353393.4:n.6274-113_6274-112del
ENST00000360256.8:c.6274-113_6274-112del	ENSP00000353393.4:n.6274-113_6274-112del
NM_000132.3:c.6274-113_6274-112del	NP_000123.1:n.6274-113_6274-112del
XM_011531126.1:c.6169-113_6169-112del	XP_011529428.1:n.6169-113_6169-112del
NM_000132.4:c.6274-113_6274-112del MANE Select	NP_000123.1:n.6274-113_6274-112del