Canonical Allele Identifier: CA873369605

Gene: F8

Linked Data

• dbSNP Id: rs1382036040
• MyVariant Identifiers: chrX:g.154863202del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863202del , CM000685.2:g.154863202del	GRCh38
NC_000023.10:g.154091477del , CM000685.1:g.154091477del	GRCh37
NC_000023.9:g.153744671del	NCBI36
NG_011403.1:g.164522del
NG_011403.2:g.164522del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6455del MANE Select	ENSP00000353393.4:p.Ser2152LeufsTer3
ENST00000644698.1:c.188del	ENSP00000495706.1:p.Ser63LeufsTer3
ENST00000330287.10:c.50del	ENSP00000327895.6:p.Ser17LeufsTer3
ENST00000360256.8:c.6455del	ENSP00000353393.4:p.Ser2152LeufsTer3
NM_000132.3:c.6455del	NP_000123.1:p.Ser2152LeufsTer3
NM_019863.2:c.50del	NP_063916.1:p.Ser17LeufsTer3
XM_011531126.1:c.6350del	XP_011529428.1:p.Ser2117LeufsTer3
NM_000132.4:c.6455del MANE Select	NP_000123.1:p.Ser2152LeufsTer3
NM_019863.3:c.50del	NP_063916.1:p.Ser17LeufsTer3