Canonical Allele Identifier: CA2466807468

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837745_154837746delinsTG , CM000685.2:g.154837745_154837746delinsTG	GRCh38
NC_000023.10:g.154066020_154066021delinsTG , CM000685.1:g.154066020_154066021delinsTG	GRCh37
NC_000023.9:g.153719214_153719215delinsTG	NCBI36
NG_011403.1:g.189978_189979delinsCA
NG_033065.1:g.1917_1918delinsCA
NG_011403.2:g.189978_189979delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6907_6908delinsCA MANE Select	ENSP00000353393.4:p.Gln2303=
ENST00000644698.1:c.640_641delinsCA	ENSP00000495706.1:p.Gln214=
ENST00000330287.10:c.502_503delinsCA	ENSP00000327895.6:p.Gln168=
ENST00000360256.8:c.6907_6908delinsCA	ENSP00000353393.4:p.Gln2303=
NM_000132.3:c.6907_6908delinsCA	NP_000123.1:p.Gln2303=
NM_019863.2:c.502_503delinsCA	NP_063916.1:p.Gln168=
XM_011531126.1:c.6802_6803delinsCA	XP_011529428.1:p.Gln2268=
NM_000132.4:c.6907_6908delinsCA MANE Select	NP_000123.1:p.Gln2303=
NM_019863.3:c.502_503delinsCA	NP_063916.1:p.Gln168=