Canonical Allele Identifier: CA2695237911

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902196_154902201del , CM000685.2:g.154902196_154902201del	GRCh38
NC_000023.10:g.154130471_154130476del , CM000685.1:g.154130471_154130476del	GRCh37
NC_000023.9:g.153783665_153783670del	NCBI36
NG_011403.1:g.125524_125529del
NG_011403.2:g.125524_125529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-33_5999-28del MANE Select	ENSP00000353393.4:n.5999-33_5999-28del
ENST00000360256.8:c.5999-33_5999-28del	ENSP00000353393.4:n.5999-33_5999-28del
NM_000132.3:c.5999-33_5999-28del	NP_000123.1:n.5999-33_5999-28del
XM_011531126.1:c.5894-33_5894-28del	XP_011529428.1:n.5894-33_5894-28del
NM_000132.4:c.5999-33_5999-28del MANE Select	NP_000123.1:n.5999-33_5999-28del