Canonical Allele Identifier: CA2695152114

Gene: F8

Linked Data

• gnomAD v4: X-154896340-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896341del , CM000685.2:g.154896341del	GRCh38
NC_000023.10:g.154124616del , CM000685.1:g.154124616del	GRCh37
NC_000023.9:g.153777810del	NCBI36
NG_011403.1:g.131383del
NG_011403.2:g.131383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-109del MANE Select	ENSP00000353393.4:n.6274-109del
ENST00000360256.8:c.6274-109del	ENSP00000353393.4:n.6274-109del
NM_000132.3:c.6274-109del	NP_000123.1:n.6274-109del
XM_011531126.1:c.6169-109del	XP_011529428.1:n.6169-109del
NM_000132.4:c.6274-109del MANE Select	NP_000123.1:n.6274-109del