Canonical Allele Identifier: CA2695237171

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863160del , CM000685.2:g.154863160del	GRCh38
NC_000023.10:g.154091435del , CM000685.1:g.154091435del	GRCh37
NC_000023.9:g.153744629del	NCBI36
NG_011403.1:g.164564del
NG_011403.2:g.164564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6497del MANE Select	ENSP00000353393.4:p.Arg2166HisfsTer20
ENST00000644698.1:c.230del	ENSP00000495706.1:p.Arg77HisfsTer20
ENST00000330287.10:c.92del	ENSP00000327895.6:p.Arg31HisfsTer20
ENST00000360256.8:c.6497del	ENSP00000353393.4:p.Arg2166HisfsTer20
NM_000132.3:c.6497del	NP_000123.1:p.Arg2166HisfsTer20
NM_019863.2:c.92del	NP_063916.1:p.Arg31HisfsTer20
XM_011531126.1:c.6392del	XP_011529428.1:p.Arg2131HisfsTer20
NM_000132.4:c.6497del MANE Select	NP_000123.1:p.Arg2166HisfsTer20
NM_019863.3:c.92del	NP_063916.1:p.Arg31HisfsTer20