Canonical Allele Identifier: CA2695237905

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902168_154902169del , CM000685.2:g.154902168_154902169del	GRCh38
NC_000023.10:g.154130443_154130444del , CM000685.1:g.154130443_154130444del	GRCh37
NC_000023.9:g.153783637_153783638del	NCBI36
NG_011403.1:g.125555_125556del
NG_011403.2:g.125555_125556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-2_5999-1del MANE Select	ENSP00000353393.4:n.5999-2_5999-1del
ENST00000360256.8:c.5999-2_5999-1del	ENSP00000353393.4:n.5999-2_5999-1del
NM_000132.3:c.5999-2_5999-1del	NP_000123.1:n.5999-2_5999-1del
XM_011531126.1:c.5894-2_5894-1del	XP_011529428.1:n.5894-2_5894-1del
NM_000132.4:c.5999-2_5999-1del MANE Select	NP_000123.1:n.5999-2_5999-1del