Canonical Allele Identifier: CA2695238442

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154992933_154992934insG , CM000685.2:g.154992933_154992934insG	GRCh38
NC_000023.10:g.154221208_154221209insG , CM000685.1:g.154221208_154221209insG	GRCh37
NC_000023.9:g.153874402_153874403insG	NCBI36
NG_011403.1:g.34790_34791insC
NG_011403.2:g.34790_34791insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.601+2_601+3insC MANE Select	ENSP00000353393.4:n.601+2_601+3insC
ENST00000647125.1:c.*387+2_*387+3insC	ENSP00000496062.1:n.*387+2_*387+3insC
ENST00000360256.8:c.601+2_601+3insC	ENSP00000353393.4:n.601+2_601+3insC
ENST00000423959.5:c.496+2_496+3insC	ENSP00000409446.1:n.496+2_496+3insC
NM_000132.3:c.601+2_601+3insC	NP_000123.1:n.601+2_601+3insC
XM_011531126.1:c.496+2_496+3insC	XP_011529428.1:n.496+2_496+3insC
NM_000132.4:c.601+2_601+3insC MANE Select	NP_000123.1:n.601+2_601+3insC