Canonical Allele Identifier: CA2695237167

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863135del , CM000685.2:g.154863135del	GRCh38
NC_000023.10:g.154091410del , CM000685.1:g.154091410del	GRCh37
NC_000023.9:g.153744604del	NCBI36
NG_011403.1:g.164590del
NG_011403.2:g.164590del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6523del MANE Select	ENSP00000353393.4:p.Tyr2175IlefsTer11
ENST00000644698.1:c.256del	ENSP00000495706.1:p.Tyr86IlefsTer11
ENST00000330287.10:c.118del	ENSP00000327895.6:p.Tyr40IlefsTer11
ENST00000360256.8:c.6523del	ENSP00000353393.4:p.Tyr2175IlefsTer11
NM_000132.3:c.6523del	NP_000123.1:p.Tyr2175IlefsTer11
NM_019863.2:c.118del	NP_063916.1:p.Tyr40IlefsTer11
XM_011531126.1:c.6418del	XP_011529428.1:p.Tyr2140IlefsTer11
NM_000132.4:c.6523del MANE Select	NP_000123.1:p.Tyr2175IlefsTer11
NM_019863.3:c.118del	NP_063916.1:p.Tyr40IlefsTer11