Canonical Allele Identifier: CA2695168092

Gene: F8

Linked Data

• gnomAD v4: X-154904630-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904634_154904635del , CM000685.2:g.154904634_154904635del	GRCh38
NC_000023.10:g.154132909_154132910del , CM000685.1:g.154132909_154132910del	GRCh37
NC_000023.9:g.153786103_153786104del	NCBI36
NG_011403.1:g.123092_123093del
NG_011403.2:g.123092_123093del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5587-108_5587-107del MANE Select	ENSP00000353393.4:n.5587-108_5587-107del
ENST00000360256.8:c.5587-108_5587-107del	ENSP00000353393.4:n.5587-108_5587-107del
NM_000132.3:c.5587-108_5587-107del	NP_000123.1:n.5587-108_5587-107del
XM_011531126.1:c.5482-108_5482-107del	XP_011529428.1:n.5482-108_5482-107del
NM_000132.4:c.5587-108_5587-107del MANE Select	NP_000123.1:n.5587-108_5587-107del