Canonical Allele Identifier: CA2824314862

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904160_154904166dup , CM000685.2:g.154904160_154904166dup	GRCh38
NC_000023.10:g.154132435_154132441dup , CM000685.1:g.154132435_154132441dup	GRCh37
NC_000023.9:g.153785629_153785635dup	NCBI36
NG_011403.1:g.123559_123565dup
NG_011403.2:g.123559_123565dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-77_5816-71dup MANE Select	ENSP00000353393.4:n.5816-77_5816-71dup
ENST00000360256.8:c.5816-77_5816-71dup	ENSP00000353393.4:n.5816-77_5816-71dup
NM_000132.3:c.5816-77_5816-71dup	NP_000123.1:n.5816-77_5816-71dup
XM_011531126.1:c.5711-77_5711-71dup	XP_011529428.1:n.5711-77_5711-71dup
NM_000132.4:c.5816-77_5816-71dup MANE Select	NP_000123.1:n.5816-77_5816-71dup