Canonical Allele Identifier: CA2695237907

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902190_154902191del , CM000685.2:g.154902190_154902191del	GRCh38
NC_000023.10:g.154130465_154130466del , CM000685.1:g.154130465_154130466del	GRCh37
NC_000023.9:g.153783659_153783660del	NCBI36
NG_011403.1:g.125534_125535del
NG_011403.2:g.125534_125535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-23_5999-22del MANE Select	ENSP00000353393.4:n.5999-23_5999-22del
ENST00000360256.8:c.5999-23_5999-22del	ENSP00000353393.4:n.5999-23_5999-22del
NM_000132.3:c.5999-23_5999-22del	NP_000123.1:n.5999-23_5999-22del
XM_011531126.1:c.5894-23_5894-22del	XP_011529428.1:n.5894-23_5894-22del
NM_000132.4:c.5999-23_5999-22del MANE Select	NP_000123.1:n.5999-23_5999-22del