Canonical Allele Identifier: CA2695237127

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860471del , CM000685.2:g.154860471del	GRCh38
NC_000023.10:g.154088746del , CM000685.1:g.154088746del	GRCh37
NC_000023.9:g.153741940del	NCBI36
NG_011403.1:g.167254del
NG_011403.2:g.167254del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6862del MANE Select	ENSP00000353393.4:p.His2288IlefsTer12
ENST00000644698.1:c.595del	ENSP00000495706.1:p.His199IlefsTer12
ENST00000330287.10:c.457del	ENSP00000327895.6:p.His153IlefsTer12
ENST00000360256.8:c.6862del	ENSP00000353393.4:p.His2288IlefsTer12
NM_000132.3:c.6862del	NP_000123.1:p.His2288IlefsTer12
NM_019863.2:c.457del	NP_063916.1:p.His153IlefsTer12
XM_011531126.1:c.6757del	XP_011529428.1:p.His2253IlefsTer12
NM_000132.4:c.6862del MANE Select	NP_000123.1:p.His2288IlefsTer12
NM_019863.3:c.457del	NP_063916.1:p.His153IlefsTer12