Canonical Allele Identifier: CA2579744888

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993216del , CM000685.2:g.154993216del	GRCh38
NC_000023.10:g.154221491del , CM000685.1:g.154221491del	GRCh37
NC_000023.9:g.153874685del	NCBI36
NG_011403.1:g.34510del
NG_011403.2:g.34510del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-66del MANE Select	ENSP00000353393.4:n.389-66del
ENST00000647125.1:c.*175-66del	ENSP00000496062.1:n.*175-66del
ENST00000360256.8:c.389-66del	ENSP00000353393.4:n.389-66del
ENST00000423959.5:c.284-66del	ENSP00000409446.1:n.284-66del
ENST00000453950.1:c.371-66del	ENSP00000389153.1:n.371-66del
NM_000132.3:c.389-66del	NP_000123.1:n.389-66del
XM_011531126.1:c.284-66del	XP_011529428.1:n.284-66del
NM_000132.4:c.389-66del MANE Select	NP_000123.1:n.389-66del