Canonical Allele Identifier: CA2120141917

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118486G= , CM000675.2:g.113118486G=	GRCh38
NC_000013.10:g.113772800G= , CM000675.1:g.113772800G=	GRCh37
NC_000013.9:g.112820801G=	NCBI36
NG_009258.1:g.688G= , LRG_548:g.688G=
NG_009262.1:g.17696G= , LRG_554:g.17696G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.813G= MANE Select	ENSP00000329546.4:p.Thr271=
ENST00000346342.7:c.813G=	ENSP00000329546.3:p.Thr271=
ENST00000375581.3:c.879G=	ENSP00000364731.3:p.Thr293=
ENST00000541084.5:c.627G=	ENSP00000442051.2:p.Thr209=
NM_000131.4:c.879G= , LRG_554t1:c.879G=	NP_000122.1:p.Thr293=
NM_001267554.1:c.627G=	NP_001254483.1:p.Thr209=
NM_019616.3:c.813G= , LRG_554t2:c.813G=	NP_062562.1:p.Thr271=
NR_051961.1:n.900G=
XM_006719963.2:c.672G=	XP_006720026.1:p.Thr224=
XM_011537474.1:c.921G=	XP_011535776.1:p.Thr307=
XM_011537475.1:c.735G=	XP_011535777.1:p.Thr245=
XM_011537476.1:c.573G=	XP_011535778.1:p.Thr191=
XM_011537477.1:c.882G=	XP_011535779.1:p.Thr294=
XM_006719963.3:c.717G=	XP_006720026.2:p.Thr239=
XM_011537474.2:c.966G=	XP_011535776.2:p.Thr322=
XM_011537475.2:c.780G=	XP_011535777.2:p.Thr260=
XM_011537476.2:c.573G=	XP_011535778.1:p.Thr191=
NM_019616.4:c.813G= MANE Select	NP_062562.1:p.Thr271=
NR_051961.2:n.897G=
NM_001267554.2:c.627G=	NP_001254483.1:p.Thr209=