Canonical Allele Identifier: CA2466807466

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837736_154837737delinsTG , CM000685.2:g.154837736_154837737delinsTG	GRCh38
NC_000023.10:g.154066011_154066012delinsTG , CM000685.1:g.154066011_154066012delinsTG	GRCh37
NC_000023.9:g.153719205_153719206delinsTG	NCBI36
NG_011403.1:g.189987_189988delinsCA
NG_033065.1:g.1926_1927delinsCA
NG_011403.2:g.189987_189988delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6916_6917delinsCA MANE Select	ENSP00000353393.4:p.Gln2306=
ENST00000644698.1:c.649_650delinsCA	ENSP00000495706.1:p.Gln217=
ENST00000330287.10:c.511_512delinsCA	ENSP00000327895.6:p.Gln171=
ENST00000360256.8:c.6916_6917delinsCA	ENSP00000353393.4:p.Gln2306=
NM_000132.3:c.6916_6917delinsCA	NP_000123.1:p.Gln2306=
NM_019863.2:c.511_512delinsCA	NP_063916.1:p.Gln171=
XM_011531126.1:c.6811_6812delinsCA	XP_011529428.1:p.Gln2271=
NM_000132.4:c.6916_6917delinsCA MANE Select	NP_000123.1:p.Gln2306=
NM_019863.3:c.511_512delinsCA	NP_063916.1:p.Gln171=