Canonical Allele Identifier: CA2120135611

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113902G= , CM000675.2:g.113113902G=	GRCh38
NC_000013.10:g.113768216G= , CM000675.1:g.113768216G=	GRCh37
NC_000013.9:g.112816217G=	NCBI36
NG_009262.1:g.13112G= , LRG_554:g.13112G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.306G= MANE Select	ENSP00000329546.4:p.Gln102=
ENST00000346342.7:c.306G=	ENSP00000329546.3:p.Gln102=
ENST00000375581.3:c.372G=	ENSP00000364731.3:p.Gln124=
ENST00000444337.1:c.*114G=	ENSP00000387669.1:n.*114G=
ENST00000473085.1:n.253G=
ENST00000479674.1:n.639G=
ENST00000541084.5:c.120G=	ENSP00000442051.2:p.Gln40=
NM_000131.4:c.372G= , LRG_554t1:c.372G=	NP_000122.1:p.Gln124=
NM_001267554.1:c.120G=	NP_001254483.1:p.Gln40=
NM_019616.3:c.306G= , LRG_554t2:c.306G=	NP_062562.1:p.Gln102=
NR_051961.1:n.393G=
XM_006719963.2:c.306G=	XP_006720026.1:p.Gln102=
XM_011537474.1:c.306G=	XP_011535776.1:p.Gln102=
XM_011537475.1:c.120G=	XP_011535777.1:p.Gln40=
XM_011537477.1:c.267G=	XP_011535779.1:p.Gln89=
XM_006719963.3:c.351G=	XP_006720026.2:p.Gln117=
XM_011537474.2:c.351G=	XP_011535776.2:p.Gln117=
XM_011537475.2:c.165G=	XP_011535777.2:p.Gln55=
NM_019616.4:c.306G= MANE Select	NP_062562.1:p.Gln102=
NR_051961.2:n.390G=
NM_001267554.2:c.120G=	NP_001254483.1:p.Gln40=