Canonical Allele Identifier: CA2466807417

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837604A= , CM000685.2:g.154837604A=	GRCh38
NC_000023.10:g.154065879A= , CM000685.1:g.154065879A=	GRCh37
NC_000023.9:g.153719073A=	NCBI36
NG_011403.1:g.190120T=
NG_033065.1:g.2059T=
NG_011403.2:g.190120T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.7049T= MANE Select	ENSP00000353393.4:p.Leu2350=
ENST00000644698.1:c.782T=	ENSP00000495706.1:p.Leu261=
ENST00000330287.10:c.644T=	ENSP00000327895.6:p.Leu215=
ENST00000360256.8:c.7049T=	ENSP00000353393.4:p.Leu2350=
NM_000132.3:c.7049T=	NP_000123.1:p.Leu2350=
NM_019863.2:c.644T=	NP_063916.1:p.Leu215=
XM_011531126.1:c.6944T=	XP_011529428.1:p.Leu2315=
NM_000132.4:c.7049T= MANE Select	NP_000123.1:p.Leu2350=
NM_019863.3:c.644T=	NP_063916.1:p.Leu215=