Canonical Allele Identifier: CA2466857757

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996981_154996982delinsGC , CM000685.2:g.154996981_154996982delinsGC	GRCh38
NC_000023.10:g.154225256_154225257delinsGC , CM000685.1:g.154225256_154225257delinsGC	GRCh37
NC_000023.9:g.153878450_153878451delinsGC	NCBI36
NG_011403.1:g.30742_30743delinsGC
NG_011403.2:g.30742_30743delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.379_380delinsGC MANE Select	ENSP00000353393.4:p.Ala127=
ENST00000647125.1:c.*165_*166delinsGC	ENSP00000496062.1:n.*165_*166delinsGC
ENST00000360256.8:c.379_380delinsGC	ENSP00000353393.4:p.Ala127=
ENST00000423959.5:c.274_275delinsGC	ENSP00000409446.1:p.Ala92=
ENST00000453950.1:c.361_362delinsGC	ENSP00000389153.1:p.Ala121=
NM_000132.3:c.379_380delinsGC	NP_000123.1:p.Ala127=
XM_011531126.1:c.274_275delinsGC	XP_011529428.1:p.Ala92=
NM_000132.4:c.379_380delinsGC MANE Select	NP_000123.1:p.Ala127=