Canonical Allele Identifier: CA2824314858

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903950_154903956del , CM000685.2:g.154903950_154903956del	GRCh38
NC_000023.10:g.154132225_154132231del , CM000685.1:g.154132225_154132231del	GRCh37
NC_000023.9:g.153785419_153785425del	NCBI36
NG_011403.1:g.123768_123774del
NG_011403.2:g.123768_123774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5948_5954del MANE Select	ENSP00000353393.4:p.Thr1983LysfsTer?
ENST00000360256.8:c.5948_5954del	ENSP00000353393.4:p.Thr1983LysfsTer?
NM_000132.3:c.5948_5954del	NP_000123.1:p.Thr1983LysfsTer?
XM_011531126.1:c.5843_5849del	XP_011529428.1:p.Thr1948LysfsTer?
NM_000132.4:c.5948_5954del MANE Select	NP_000123.1:p.Thr1983LysfsTer?