Canonical Allele Identifier: CA2570585022

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863024_154863025del , CM000685.2:g.154863024_154863025del	GRCh38
NC_000023.10:g.154091299_154091300del , CM000685.1:g.154091299_154091300del	GRCh37
NC_000023.9:g.153744493_153744494del	NCBI36
NG_011403.1:g.164700_164701del
NG_011403.2:g.164700_164701del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6574+59_6574+60del MANE Select	ENSP00000353393.4:n.6574+59_6574+60del
ENST00000644698.1:c.307+59_307+60del	ENSP00000495706.1:n.307+59_307+60del
ENST00000330287.10:c.169+59_169+60del	ENSP00000327895.6:n.169+59_169+60del
ENST00000360256.8:c.6574+59_6574+60del	ENSP00000353393.4:n.6574+59_6574+60del
NM_000132.3:c.6574+59_6574+60del	NP_000123.1:n.6574+59_6574+60del
NM_019863.2:c.169+59_169+60del	NP_063916.1:n.169+59_169+60del
XM_011531126.1:c.6469+59_6469+60del	XP_011529428.1:n.6469+59_6469+60del
NM_000132.4:c.6574+59_6574+60del MANE Select	NP_000123.1:n.6574+59_6574+60del
NM_019863.3:c.169+59_169+60del	NP_063916.1:n.169+59_169+60del