Canonical Allele Identifier: CA2466815010

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860536_154860538delinsCCT , CM000685.2:g.154860536_154860538delinsCCT	GRCh38
NC_000023.10:g.154088811_154088813delinsCCT , CM000685.1:g.154088811_154088813delinsCCT	GRCh37
NC_000023.9:g.153742005_153742007delinsCCT	NCBI36
NG_011403.1:g.167186_167188delinsAGG
NG_011403.2:g.167186_167188delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6794_6796delinsAGG MANE Select	ENSP00000353393.4:p.Gln2265=
ENST00000644698.1:c.527_529delinsAGG	ENSP00000495706.1:p.Gln176=
ENST00000330287.10:c.389_391delinsAGG	ENSP00000327895.6:p.Gln130=
ENST00000360256.8:c.6794_6796delinsAGG	ENSP00000353393.4:p.Gln2265=
NM_000132.3:c.6794_6796delinsAGG	NP_000123.1:p.Gln2265=
NM_019863.2:c.389_391delinsAGG	NP_063916.1:p.Gln130=
XM_011531126.1:c.6689_6691delinsAGG	XP_011529428.1:p.Gln2230=
NM_000132.4:c.6794_6796delinsAGG MANE Select	NP_000123.1:p.Gln2265=
NM_019863.3:c.389_391delinsAGG	NP_063916.1:p.Gln130=