Canonical Allele Identifier: CA2466844385

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954085_154954088delinsATGT , CM000685.2:g.154954085_154954088delinsATGT	GRCh38
NC_000023.10:g.154182360_154182363delinsATGT , CM000685.1:g.154182360_154182363delinsATGT	GRCh37
NC_000023.9:g.153835554_153835557delinsATGT	NCBI36
NG_011403.1:g.73636_73639delinsACAT
NG_011403.2:g.73636_73639delinsACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-46_1753-43delinsACAT MANE Select	ENSP00000353393.4:n.1753-46_1753-43delinsACAT
ENST00000647125.1:c.*1629-46_*1629-43delinsACAT	ENSP00000496062.1:n.*1629-46_*1629-43delinsACAT
ENST00000360256.8:c.1753-46_1753-43delinsACAT	ENSP00000353393.4:n.1753-46_1753-43delinsACAT
NM_000132.3:c.1753-46_1753-43delinsACAT	NP_000123.1:n.1753-46_1753-43delinsACAT
XM_011531126.1:c.1648-46_1648-43delinsACAT	XP_011529428.1:n.1648-46_1648-43delinsACAT
NM_000132.4:c.1753-46_1753-43delinsACAT MANE Select	NP_000123.1:n.1753-46_1753-43delinsACAT