Canonical Allele Identifier: CA2695237925

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903928_154903931del , CM000685.2:g.154903928_154903931del	GRCh38
NC_000023.10:g.154132203_154132206del , CM000685.1:g.154132203_154132206del	GRCh37
NC_000023.9:g.153785397_153785400del	NCBI36
NG_011403.1:g.123793_123796del
NG_011403.2:g.123793_123796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5973_5976del MANE Select	ENSP00000353393.4:p.Met1992HisfsTer?
ENST00000360256.8:c.5973_5976del	ENSP00000353393.4:p.Met1992HisfsTer?
NM_000132.3:c.5973_5976del	NP_000123.1:p.Met1992HisfsTer?
XM_011531126.1:c.5868_5871del	XP_011529428.1:p.Met1957HisfsTer?
NM_000132.4:c.5973_5976del MANE Select	NP_000123.1:p.Met1992HisfsTer?