Canonical Allele Identifier: CA2466857823

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997135_154997136delinsAG , CM000685.2:g.154997135_154997136delinsAG	GRCh38
NC_000023.10:g.154225410_154225411delinsAG , CM000685.1:g.154225410_154225411delinsAG	GRCh37
NC_000023.9:g.153878604_153878605delinsAG	NCBI36
NG_011403.1:g.30588_30589delinsCT
NG_011403.2:g.30588_30589delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.266-41_266-40delinsCT MANE Select	ENSP00000353393.4:n.266-41_266-40delinsCT...
ENST00000647125.1:c.*52-41_*52-40delinsCT	ENSP00000496062.1:n.*52-41_*52-40delinsCT...
ENST00000360256.8:c.266-41_266-40delinsCT	ENSP00000353393.4:n.266-41_266-40delinsCT...
ENST00000423959.5:c.161-41_161-40delinsCT	ENSP00000409446.1:n.161-41_161-40delinsCT...
ENST00000453950.1:c.248-41_248-40delinsCT	ENSP00000389153.1:n.248-41_248-40delinsCT...
NM_000132.3:c.266-41_266-40delinsCT	NP_000123.1:n.266-41_266-40delinsCT
XM_011531126.1:c.161-41_161-40delinsCT	XP_011529428.1:n.161-41_161-40delinsCT
NM_000132.4:c.266-41_266-40delinsCT MANE Select	NP_000123.1:n.266-41_266-40delinsCT