Canonical Allele Identifier: CA2541556227

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957353_154957354del , CM000685.2:g.154957353_154957354del	GRCh38
NC_000023.10:g.154185628_154185629del , CM000685.1:g.154185628_154185629del	GRCh37
NC_000023.9:g.153838822_153838823del	NCBI36
NG_011403.1:g.70373_70374del
NG_011403.2:g.70373_70374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-180_1538-179del MANE Select	ENSP00000353393.4:n.1538-180_1538-179del
ENST00000647125.1:c.*1414-180_*1414-179del	ENSP00000496062.1:n.*1414-180_*1414-179del
ENST00000360256.8:c.1538-180_1538-179del	ENSP00000353393.4:n.1538-180_1538-179del
NM_000132.3:c.1538-180_1538-179del	NP_000123.1:n.1538-180_1538-179del
XM_011531126.1:c.1433-180_1433-179del	XP_011529428.1:n.1433-180_1433-179del
NM_000132.4:c.1538-180_1538-179del MANE Select	NP_000123.1:n.1538-180_1538-179del