Canonical Allele Identifier: CA2120141654

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118421G= , CM000675.2:g.113118421G=	GRCh38
NC_000013.10:g.113772735G= , CM000675.1:g.113772735G=	GRCh37
NC_000013.9:g.112820736G=	NCBI36
NG_009258.1:g.623G= , LRG_548:g.623G=
NG_009262.1:g.17631G= , LRG_554:g.17631G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.748G= MANE Select	ENSP00000329546.4:p.Asp250=
ENST00000346342.7:c.748G=	ENSP00000329546.3:p.Asp250=
ENST00000375581.3:c.814G=	ENSP00000364731.3:p.Asp272=
ENST00000541084.5:c.562G=	ENSP00000442051.2:p.Asp188=
NM_000131.4:c.814G= , LRG_554t1:c.814G=	NP_000122.1:p.Asp272=
NM_001267554.1:c.562G=	NP_001254483.1:p.Asp188=
NM_019616.3:c.748G= , LRG_554t2:c.748G=	NP_062562.1:p.Asp250=
NR_051961.1:n.835G=
XM_006719963.2:c.607G=	XP_006720026.1:p.Asp203=
XM_011537474.1:c.856G=	XP_011535776.1:p.Asp286=
XM_011537475.1:c.670G=	XP_011535777.1:p.Asp224=
XM_011537476.1:c.508G=	XP_011535778.1:p.Asp170=
XM_011537477.1:c.817G=	XP_011535779.1:p.Asp273=
XM_006719963.3:c.652G=	XP_006720026.2:p.Asp218=
XM_011537474.2:c.901G=	XP_011535776.2:p.Asp301=
XM_011537475.2:c.715G=	XP_011535777.2:p.Asp239=
XM_011537476.2:c.508G=	XP_011535778.1:p.Asp170=
NM_019616.4:c.748G= MANE Select	NP_062562.1:p.Asp250=
NR_051961.2:n.832G=
NM_001267554.2:c.562G=	NP_001254483.1:p.Asp188=