Canonical Allele Identifier: CA2695153022

Gene: F8

Linked Data

• gnomAD v4: X-154903884-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903887_154903888del , CM000685.2:g.154903887_154903888del	GRCh38
NC_000023.10:g.154132162_154132163del , CM000685.1:g.154132162_154132163del	GRCh37
NC_000023.9:g.153785356_153785357del	NCBI36
NG_011403.1:g.123838_123839del
NG_011403.2:g.123838_123839del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5998+20_5998+21del MANE Select	ENSP00000353393.4:n.5998+20_5998+21del
ENST00000360256.8:c.5998+20_5998+21del	ENSP00000353393.4:n.5998+20_5998+21del
NM_000132.3:c.5998+20_5998+21del	NP_000123.1:n.5998+20_5998+21del
XM_011531126.1:c.5893+20_5893+21del	XP_011529428.1:n.5893+20_5893+21del
NM_000132.4:c.5998+20_5998+21del MANE Select	NP_000123.1:n.5998+20_5998+21del