Canonical Allele Identifier: CA2695237166

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863121del , CM000685.2:g.154863121del	GRCh38
NC_000023.10:g.154091396del , CM000685.1:g.154091396del	GRCh37
NC_000023.9:g.153744590del	NCBI36
NG_011403.1:g.164603del
NG_011403.2:g.164603del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6536del MANE Select	ENSP00000353393.4:p.Ser2179ThrfsTer7
ENST00000644698.1:c.269del	ENSP00000495706.1:p.Ser90ThrfsTer7
ENST00000330287.10:c.131del	ENSP00000327895.6:p.Ser44ThrfsTer7
ENST00000360256.8:c.6536del	ENSP00000353393.4:p.Ser2179ThrfsTer7
NM_000132.3:c.6536del	NP_000123.1:p.Ser2179ThrfsTer7
NM_019863.2:c.131del	NP_063916.1:p.Ser44ThrfsTer7
XM_011531126.1:c.6431del	XP_011529428.1:p.Ser2144ThrfsTer7
NM_000132.4:c.6536del MANE Select	NP_000123.1:p.Ser2179ThrfsTer7
NM_019863.3:c.131del	NP_063916.1:p.Ser44ThrfsTer7