Canonical Allele Identifier: CA2695237168

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863138_154863140dup , CM000685.2:g.154863138_154863140dup	GRCh38
NC_000023.10:g.154091413_154091415dup , CM000685.1:g.154091413_154091415dup	GRCh37
NC_000023.9:g.153744607_153744609dup	NCBI36
NG_011403.1:g.164584_164586dup
NG_011403.2:g.164584_164586dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6517_6519dup MANE Select	ENSP00000353393.4:p.Thr2173_His2174insThr
ENST00000644698.1:c.250_252dup	ENSP00000495706.1:p.Thr84_His85insThr
ENST00000330287.10:c.112_114dup	ENSP00000327895.6:p.Thr38_His39insThr
ENST00000360256.8:c.6517_6519dup	ENSP00000353393.4:p.Thr2173_His2174insThr
NM_000132.3:c.6517_6519dup	NP_000123.1:p.Thr2173_His2174insThr
NM_019863.2:c.112_114dup	NP_063916.1:p.Thr38_His39insThr
XM_011531126.1:c.6412_6414dup	XP_011529428.1:p.Thr2138_His2139insThr
NM_000132.4:c.6517_6519dup MANE Select	NP_000123.1:p.Thr2173_His2174insThr
NM_019863.3:c.112_114dup	NP_063916.1:p.Thr38_His39insThr