Canonical Allele Identifier: CA2695237110

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837673_154837681del , CM000685.2:g.154837673_154837681del	GRCh38
NC_000023.10:g.154065948_154065956del , CM000685.1:g.154065948_154065956del	GRCh37
NC_000023.9:g.153719142_153719150del	NCBI36
NG_011403.1:g.190043_190051del
NG_033065.1:g.1982_1990del
NG_011403.2:g.190043_190051del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6972_6980del MANE Select	ENSP00000353393.4:p.Leu2325_Ile2327del
ENST00000644698.1:c.705_713del	ENSP00000495706.1:p.Leu236_Ile238del
ENST00000330287.10:c.567_575del	ENSP00000327895.6:p.Leu190_Ile192del
ENST00000360256.8:c.6972_6980del	ENSP00000353393.4:p.Leu2325_Ile2327del
NM_000132.3:c.6972_6980del	NP_000123.1:p.Leu2325_Ile2327del
NM_019863.2:c.567_575del	NP_063916.1:p.Leu190_Ile192del
XM_011531126.1:c.6867_6875del	XP_011529428.1:p.Leu2290_Ile2292del
NM_000132.4:c.6972_6980del MANE Select	NP_000123.1:p.Leu2325_Ile2327del
NM_019863.3:c.567_575del	NP_063916.1:p.Leu190_Ile192del