Canonical Allele Identifier: CA2018007884

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118501C= , CM000675.2:g.113118501C=	GRCh38
NC_000013.10:g.113772815C= , CM000675.1:g.113772815C=	GRCh37
NC_000013.9:g.112820816C=	NCBI36
NG_009258.1:g.703C= , LRG_548:g.703C=
NG_009262.1:g.17711C= , LRG_554:g.17711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.828C= MANE Select	ENSP00000329546.4:p.Thr276=
ENST00000346342.7:c.828C=	ENSP00000329546.3:p.Thr276=
ENST00000375581.3:c.894C=	ENSP00000364731.3:p.Thr298=
ENST00000541084.5:c.642C=	ENSP00000442051.2:p.Thr214=
NM_000131.4:c.894C= , LRG_554t1:c.894C=	NP_000122.1:p.Thr298=
NM_001267554.1:c.642C=	NP_001254483.1:p.Thr214=
NM_019616.3:c.828C= , LRG_554t2:c.828C=	NP_062562.1:p.Thr276=
NR_051961.1:n.915C=
XM_006719963.2:c.687C=	XP_006720026.1:p.Thr229=
XM_011537474.1:c.936C=	XP_011535776.1:p.Thr312=
XM_011537475.1:c.750C=	XP_011535777.1:p.Thr250=
XM_011537476.1:c.588C=	XP_011535778.1:p.Thr196=
XM_011537477.1:c.897C=	XP_011535779.1:p.Thr299=
XM_006719963.3:c.732C=	XP_006720026.2:p.Thr244=
XM_011537474.2:c.981C=	XP_011535776.2:p.Thr327=
XM_011537475.2:c.795C=	XP_011535777.2:p.Thr265=
XM_011537476.2:c.588C=	XP_011535778.1:p.Thr196=
NM_019616.4:c.828C= MANE Select	NP_062562.1:p.Thr276=
NR_051961.2:n.912C=
NM_001267554.2:c.642C=	NP_001254483.1:p.Thr214=