Canonical Allele Identifier: CA2695237165

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863108del , CM000685.2:g.154863108del	GRCh38
NC_000023.10:g.154091383del , CM000685.1:g.154091383del	GRCh37
NC_000023.9:g.153744577del	NCBI36
NG_011403.1:g.164617del
NG_011403.2:g.164617del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6550del MANE Select	ENSP00000353393.4:p.Glu2184SerfsTer2
ENST00000644698.1:c.283del	ENSP00000495706.1:p.Glu95SerfsTer2
ENST00000330287.10:c.145del	ENSP00000327895.6:p.Glu49SerfsTer2
ENST00000360256.8:c.6550del	ENSP00000353393.4:p.Glu2184SerfsTer2
NM_000132.3:c.6550del	NP_000123.1:p.Glu2184SerfsTer2
NM_019863.2:c.145del	NP_063916.1:p.Glu49SerfsTer2
XM_011531126.1:c.6445del	XP_011529428.1:p.Glu2149SerfsTer2
NM_000132.4:c.6550del MANE Select	NP_000123.1:p.Glu2184SerfsTer2
NM_019863.3:c.145del	NP_063916.1:p.Glu49SerfsTer2