Canonical Allele Identifier: CA2579753334

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022701del , CM000685.2:g.155022701del	GRCh38
NC_000023.10:g.154250976del , CM000685.1:g.154250976del	GRCh37
NC_000023.9:g.153904170del	NCBI36
NG_011403.1:g.5023del
NG_011403.2:g.5023del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-149del MANE Select	ENSP00000353393.4:n.-149del
ENST00000647125.1:c.-149del	ENSP00000496062.1:n.-149del
ENST00000360256.8:c.-149del	ENSP00000353393.4:n.-149del
ENST00000423959.5:c.38+4079del	ENSP00000409446.1:n.38+4079del
ENST00000453950.1:c.39-205del	ENSP00000389153.1:n.39-205del
NM_000132.3:c.-149del	NP_000123.1:n.-149del
XM_011531126.1:c.38+4079del	XP_011529428.1:n.38+4079del
NM_000132.4:c.-149del MANE Select	NP_000123.1:n.-149del