Canonical Allele Identifier: CA2466865492

Gene: F8

Linked Data

• dbSNP Id: rs1557287637

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022664_155022665insAATGTTACTCTAAATAGCAAAATACA , CM000685.2:g.155022664_155022665insAATGTTACTCTAAATAGCAAAATACA	GRCh38
NC_000023.10:g.154250939_154250940insAATGTTACTCTAAATAGCAAAATACA , CM000685.1:g.154250939_154250940insAATGTTACTCTAAATAGCAAAATACA	GRCh37
NC_000023.9:g.153904133_153904134insAATGTTACTCTAAATAGCAAAATACA	NCBI36
NG_011403.1:g.5059_5060insTGTATTTTGCTATTTAGAGTAACATT
NG_011403.2:g.5059_5060insTGTATTTTGCTATTTAGAGTAACATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-113_-112insTGTATTTTGCTATTTAGAGTAACATT MANE Select	ENSP00000353393.4:n.-113_-112insTGTATTTTGCTATTTAGAGTAACATT
ENST00000647125.1:c.-113_-112insTGTATTTTGCTATTTAGAGTAACATT	ENSP00000496062.1:n.-113_-112insTGTATTTTGCTATTTAGAGTAACATT
ENST00000360256.8:c.-113_-112insTGTATTTTGCTATTTAGAGTAACATT	ENSP00000353393.4:n.-113_-112insTGTATTTTGCTATTTAGAGTAACATT
ENST00000423959.5:c.38+4115_38+4116insTGTATTTTGCTATTTAGAGTAACATT	ENSP00000409446.1:n.38+4115_38+4116insTGTATTTTGCTATTTAGAGTAAC...
ENST00000453950.1:c.39-169_39-168insTGTATTTTGCTATTTAGAGTAACATT	ENSP00000389153.1:n.39-169_39-168insTGTATTTTGCTATTTAGAGTAACAT...
NM_000132.3:c.-113_-112insTGTATTTTGCTATTTAGAGTAACATT	NP_000123.1:n.-113_-112insTGTATTTTGCTATTTAGAGTAACATT
XM_011531126.1:c.38+4115_38+4116insTGTATTTTGCTATTTAGAGTAACATT	XP_011529428.1:n.38+4115_38+4116insTGTATTTTGCTATTTAGAGTAACATT...
NM_000132.4:c.-113_-112insTGTATTTTGCTATTTAGAGTAACATT MANE Select	NP_000123.1:n.-113_-112insTGTATTTTGCTATTTAGAGTAACATT