Canonical Allele Identifier: CA2120141722

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118437A= , CM000675.2:g.113118437A=	GRCh38
NC_000013.10:g.113772751A= , CM000675.1:g.113772751A=	GRCh37
NC_000013.9:g.112820752A=	NCBI36
NG_009258.1:g.639A= , LRG_548:g.639A=
NG_009262.1:g.17647A= , LRG_554:g.17647A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.764A= MANE Select	ENSP00000329546.4:p.Asp255=
ENST00000346342.7:c.764A=	ENSP00000329546.3:p.Asp255=
ENST00000375581.3:c.830A=	ENSP00000364731.3:p.Asp277=
ENST00000541084.5:c.578A=	ENSP00000442051.2:p.Asp193=
NM_000131.4:c.830A= , LRG_554t1:c.830A=	NP_000122.1:p.Asp277=
NM_001267554.1:c.578A=	NP_001254483.1:p.Asp193=
NM_019616.3:c.764A= , LRG_554t2:c.764A=	NP_062562.1:p.Asp255=
NR_051961.1:n.851A=
XM_006719963.2:c.623A=	XP_006720026.1:p.Asp208=
XM_011537474.1:c.872A=	XP_011535776.1:p.Asp291=
XM_011537475.1:c.686A=	XP_011535777.1:p.Asp229=
XM_011537476.1:c.524A=	XP_011535778.1:p.Asp175=
XM_011537477.1:c.833A=	XP_011535779.1:p.Asp278=
XM_006719963.3:c.668A=	XP_006720026.2:p.Asp223=
XM_011537474.2:c.917A=	XP_011535776.2:p.Asp306=
XM_011537475.2:c.731A=	XP_011535777.2:p.Asp244=
XM_011537476.2:c.524A=	XP_011535778.1:p.Asp175=
NM_019616.4:c.764A= MANE Select	NP_062562.1:p.Asp255=
NR_051961.2:n.848A=
NM_001267554.2:c.578A=	NP_001254483.1:p.Asp193=