Canonical Allele Identifier: CA2579752264

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863174del , CM000685.2:g.154863174del	GRCh38
NC_000023.10:g.154091449del , CM000685.1:g.154091449del	GRCh37
NC_000023.9:g.153744643del	NCBI36
NG_011403.1:g.164550del
NG_011403.2:g.164550del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6483del MANE Select	ENSP00000353393.4:p.Pro2162GlnfsTer24
ENST00000644698.1:c.216del	ENSP00000495706.1:p.Pro73GlnfsTer24
ENST00000330287.10:c.78del	ENSP00000327895.6:p.Pro27GlnfsTer24
ENST00000360256.8:c.6483del	ENSP00000353393.4:p.Pro2162GlnfsTer24
NM_000132.3:c.6483del	NP_000123.1:p.Pro2162GlnfsTer24
NM_019863.2:c.78del	NP_063916.1:p.Pro27GlnfsTer24
XM_011531126.1:c.6378del	XP_011529428.1:p.Pro2127GlnfsTer24
NM_000132.4:c.6483del MANE Select	NP_000123.1:p.Pro2162GlnfsTer24
NM_019863.3:c.78del	NP_063916.1:p.Pro27GlnfsTer24