Canonical Allele Identifier: CA2466856591

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993199_154993201delinsAAG , CM000685.2:g.154993199_154993201delinsAAG	GRCh38
NC_000023.10:g.154221474_154221476delinsAAG , CM000685.1:g.154221474_154221476delinsAAG	GRCh37
NC_000023.9:g.153874668_153874670delinsAAG	NCBI36
NG_011403.1:g.34523_34525delinsCTT
NG_011403.2:g.34523_34525delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-53_389-51delinsCTT MANE Select	ENSP00000353393.4:n.389-53_389-51delinsCTT
ENST00000647125.1:c.*175-53_*175-51delinsCTT	ENSP00000496062.1:n.*175-53_*175-51delinsCTT
ENST00000360256.8:c.389-53_389-51delinsCTT	ENSP00000353393.4:n.389-53_389-51delinsCTT
ENST00000423959.5:c.284-53_284-51delinsCTT	ENSP00000409446.1:n.284-53_284-51delinsCTT
ENST00000453950.1:c.371-53_371-51delinsCTT	ENSP00000389153.1:n.371-53_371-51delinsCTT
NM_000132.3:c.389-53_389-51delinsCTT	NP_000123.1:n.389-53_389-51delinsCTT
XM_011531126.1:c.284-53_284-51delinsCTT	XP_011529428.1:n.284-53_284-51delinsCTT
NM_000132.4:c.389-53_389-51delinsCTT MANE Select	NP_000123.1:n.389-53_389-51delinsCTT