Canonical Allele Identifier: CA2695237101

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837599del , CM000685.2:g.154837599del	GRCh38
NC_000023.10:g.154065874del , CM000685.1:g.154065874del	GRCh37
NC_000023.9:g.153719068del	NCBI36
NG_011403.1:g.190125del
NG_033065.1:g.2064del
NG_011403.2:g.190125del

Transcript Alleles

HGVS	Amino-acid Change
NM_000132.4:c.7054del MANE Select	NP_000123.1:p.Ter2352GluextTer?
ENST00000360256.9:c.7054del MANE Select	ENSP00000353393.4:p.Ter2352GluextTer?
NM_000132.3:c.7054del	NP_000123.1:p.Ter2352GluextTer?
NM_019863.2:c.649del	NP_063916.1:p.Ter217GluextTer?
NM_019863.3:c.649del	NP_063916.1:p.Ter217GluextTer?
ENST00000330287.10:c.649del	ENSP00000327895.6:p.Ter217GluextTer?
ENST00000360256.8:c.7054del	ENSP00000353393.4:p.Ter2352GluextTer?
ENST00000644698.1:c.787del	ENSP00000495706.1:p.Ter263GluextTer?
XM_011531126.1:c.6949del	XP_011529428.1:p.Ter2317GluextTer?