Canonical Allele Identifier: CA2695237129

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860507del , CM000685.2:g.154860507del	GRCh38
NC_000023.10:g.154088782del , CM000685.1:g.154088782del	GRCh37
NC_000023.9:g.153741976del	NCBI36
NG_011403.1:g.167217del
NG_011403.2:g.167217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6825del MANE Select	ENSP00000353393.4:p.Tyr2275Ter
ENST00000644698.1:c.558del	ENSP00000495706.1:p.Tyr186Ter
ENST00000330287.10:c.420del	ENSP00000327895.6:p.Tyr140Ter
ENST00000360256.8:c.6825del	ENSP00000353393.4:p.Tyr2275Ter
NM_000132.3:c.6825del	NP_000123.1:p.Tyr2275Ter
NM_019863.2:c.420del	NP_063916.1:p.Tyr140Ter
XM_011531126.1:c.6720del	XP_011529428.1:p.Tyr2240Ter
NM_000132.4:c.6825del MANE Select	NP_000123.1:p.Tyr2275Ter
NM_019863.3:c.420del	NP_063916.1:p.Tyr140Ter