Canonical Allele Identifier: CA2695237111

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837679_154837687del , CM000685.2:g.154837679_154837687del	GRCh38
NC_000023.10:g.154065954_154065962del , CM000685.1:g.154065954_154065962del	GRCh37
NC_000023.9:g.153719148_153719156del	NCBI36
NG_011403.1:g.190040_190048del
NG_033065.1:g.1979_1987del
NG_011403.2:g.190040_190048del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6969_6977del MANE Select	ENSP00000353393.4:p.Tyr2324_Arg2326del
ENST00000644698.1:c.702_710del	ENSP00000495706.1:p.Tyr235_Arg237del
ENST00000330287.10:c.564_572del	ENSP00000327895.6:p.Tyr189_Arg191del
ENST00000360256.8:c.6969_6977del	ENSP00000353393.4:p.Tyr2324_Arg2326del
NM_000132.3:c.6969_6977del	NP_000123.1:p.Tyr2324_Arg2326del
NM_019863.2:c.564_572del	NP_063916.1:p.Tyr189_Arg191del
XM_011531126.1:c.6864_6872del	XP_011529428.1:p.Tyr2289_Arg2291del
NM_000132.4:c.6969_6977del MANE Select	NP_000123.1:p.Tyr2324_Arg2326del
NM_019863.3:c.564_572del	NP_063916.1:p.Tyr189_Arg191del