Canonical Allele Identifier: CA2695237105

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837647dup , CM000685.2:g.154837647dup	GRCh38
NC_000023.10:g.154065922dup , CM000685.1:g.154065922dup	GRCh37
NC_000023.9:g.153719116dup	NCBI36
NG_011403.1:g.190077dup
NG_033065.1:g.2016dup
NG_011403.2:g.190077dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7006dup MANE Select	ENSP00000353393.4:p.Ile2336AsnfsTer?
ENST00000644698.1:c.739dup	ENSP00000495706.1:p.Ile247AsnfsTer?
ENST00000330287.10:c.601dup	ENSP00000327895.6:p.Ile201AsnfsTer?
ENST00000360256.8:c.7006dup	ENSP00000353393.4:p.Ile2336AsnfsTer?
NM_000132.3:c.7006dup	NP_000123.1:p.Ile2336AsnfsTer?
NM_019863.2:c.601dup	NP_063916.1:p.Ile201AsnfsTer?
XM_011531126.1:c.6901dup	XP_011529428.1:p.Ile2301AsnfsTer?
NM_000132.4:c.7006dup MANE Select	NP_000123.1:p.Ile2336AsnfsTer?
NM_019863.3:c.601dup	NP_063916.1:p.Ile201AsnfsTer?