Canonical Allele Identifier: CA2824315612

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957298_154957299insAGTA , CM000685.2:g.154957298_154957299insAGTA	GRCh38
NC_000023.10:g.154185573_154185574insAGTA , CM000685.1:g.154185573_154185574insAGTA	GRCh37
NC_000023.9:g.153838767_153838768insAGTA	NCBI36
NG_011403.1:g.70425_70426insTACT
NG_011403.2:g.70425_70426insTACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-128_1538-127insTACT MANE Select	ENSP00000353393.4:n.1538-128_1538-127insTACT
ENST00000647125.1:c.*1414-128_*1414-127insTACT	ENSP00000496062.1:n.*1414-128_*1414-127insTACT
ENST00000360256.8:c.1538-128_1538-127insTACT	ENSP00000353393.4:n.1538-128_1538-127insTACT
NM_000132.3:c.1538-128_1538-127insTACT	NP_000123.1:n.1538-128_1538-127insTACT
XM_011531126.1:c.1433-128_1433-127insTACT	XP_011529428.1:n.1433-128_1433-127insTACT
NM_000132.4:c.1538-128_1538-127insTACT MANE Select	NP_000123.1:n.1538-128_1538-127insTACT