Canonical Allele Identifier: CA2466814979

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860449_154860453delinsGAAAA , CM000685.2:g.154860449_154860453delinsGAAAA	GRCh38
NC_000023.10:g.154088724_154088728delinsGAAAA , CM000685.1:g.154088724_154088728delinsGAAAA	GRCh37
NC_000023.9:g.153741918_153741922delinsGAAAA	NCBI36
NG_011403.1:g.167271_167275delinsTTTTC
NG_011403.2:g.167271_167275delinsTTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6879_6883delinsTTTTC MANE Select	ENSP00000353393.4:p.Phe2293=
ENST00000644698.1:c.612_616delinsTTTTC	ENSP00000495706.1:p.Phe204=
ENST00000330287.10:c.474_478delinsTTTTC	ENSP00000327895.6:p.Phe158=
ENST00000360256.8:c.6879_6883delinsTTTTC	ENSP00000353393.4:p.Phe2293=
NM_000132.3:c.6879_6883delinsTTTTC	NP_000123.1:p.Phe2293=
NM_019863.2:c.474_478delinsTTTTC	NP_063916.1:p.Phe158=
XM_011531126.1:c.6774_6778delinsTTTTC	XP_011529428.1:p.Phe2258=
NM_000132.4:c.6879_6883delinsTTTTC MANE Select	NP_000123.1:p.Phe2293=
NM_019863.3:c.474_478delinsTTTTC	NP_063916.1:p.Phe158=