Canonical Allele Identifier: CA2466828216

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904129_154904131delinsTAA , CM000685.2:g.154904129_154904131delinsTAA	GRCh38
NC_000023.10:g.154132404_154132406delinsTAA , CM000685.1:g.154132404_154132406delinsTAA	GRCh37
NC_000023.9:g.153785598_153785600delinsTAA	NCBI36
NG_011403.1:g.123593_123595delinsTTA
NG_011403.2:g.123593_123595delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-43_5816-41delinsTTA MANE Select	ENSP00000353393.4:n.5816-43_5816-41delinsTTA
ENST00000360256.8:c.5816-43_5816-41delinsTTA	ENSP00000353393.4:n.5816-43_5816-41delinsTTA
NM_000132.3:c.5816-43_5816-41delinsTTA	NP_000123.1:n.5816-43_5816-41delinsTTA
XM_011531126.1:c.5711-43_5711-41delinsTTA	XP_011529428.1:n.5711-43_5711-41delinsTTA
NM_000132.4:c.5816-43_5816-41delinsTTA MANE Select	NP_000123.1:n.5816-43_5816-41delinsTTA