Canonical Allele Identifier: CA2695237136

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860546_154860554del , CM000685.2:g.154860546_154860554del	GRCh38
NC_000023.10:g.154088821_154088829del , CM000685.1:g.154088821_154088829del	GRCh37
NC_000023.9:g.153742015_153742023del	NCBI36
NG_011403.1:g.167172_167180del
NG_011403.2:g.167172_167180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6780_6788del MANE Select	ENSP00000353393.4:p.Gly2261_Thr2263del
ENST00000644698.1:c.513_521del	ENSP00000495706.1:p.Gly172_Thr174del
ENST00000330287.10:c.375_383del	ENSP00000327895.6:p.Gly126_Thr128del
ENST00000360256.8:c.6780_6788del	ENSP00000353393.4:p.Gly2261_Thr2263del
NM_000132.3:c.6780_6788del	NP_000123.1:p.Gly2261_Thr2263del
NM_019863.2:c.375_383del	NP_063916.1:p.Gly126_Thr128del
XM_011531126.1:c.6675_6683del	XP_011529428.1:p.Gly2226_Thr2228del
NM_000132.4:c.6780_6788del MANE Select	NP_000123.1:p.Gly2261_Thr2263del
NM_019863.3:c.375_383del	NP_063916.1:p.Gly126_Thr128del