Canonical Allele Identifier: CA2695152118

Gene: F8

Linked Data

• gnomAD v4: X-154896346-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896347_154896349del , CM000685.2:g.154896347_154896349del	GRCh38
NC_000023.10:g.154124622_154124624del , CM000685.1:g.154124622_154124624del	GRCh37
NC_000023.9:g.153777816_153777818del	NCBI36
NG_011403.1:g.131375_131377del
NG_011403.2:g.131375_131377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-117_6274-115del MANE Select	ENSP00000353393.4:n.6274-117_6274-115del
ENST00000360256.8:c.6274-117_6274-115del	ENSP00000353393.4:n.6274-117_6274-115del
NM_000132.3:c.6274-117_6274-115del	NP_000123.1:n.6274-117_6274-115del
XM_011531126.1:c.6169-117_6169-115del	XP_011529428.1:n.6169-117_6169-115del
NM_000132.4:c.6274-117_6274-115del MANE Select	NP_000123.1:n.6274-117_6274-115del