Canonical Allele Identifier: CA2120141953

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118502A= , CM000675.2:g.113118502A=	GRCh38
NC_000013.10:g.113772816A= , CM000675.1:g.113772816A=	GRCh37
NC_000013.9:g.112820817A=	NCBI36
NG_009258.1:g.704A= , LRG_548:g.704A=
NG_009262.1:g.17712A= , LRG_554:g.17712A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.829A= MANE Select	ENSP00000329546.4:p.Thr277=
ENST00000346342.7:c.829A=	ENSP00000329546.3:p.Thr277=
ENST00000375581.3:c.895A=	ENSP00000364731.3:p.Thr299=
ENST00000541084.5:c.643A=	ENSP00000442051.2:p.Thr215=
NM_000131.4:c.895A= , LRG_554t1:c.895A=	NP_000122.1:p.Thr299=
NM_001267554.1:c.643A=	NP_001254483.1:p.Thr215=
NM_019616.3:c.829A= , LRG_554t2:c.829A=	NP_062562.1:p.Thr277=
NR_051961.1:n.916A=
XM_006719963.2:c.688A=	XP_006720026.1:p.Thr230=
XM_011537474.1:c.937A=	XP_011535776.1:p.Thr313=
XM_011537475.1:c.751A=	XP_011535777.1:p.Thr251=
XM_011537476.1:c.589A=	XP_011535778.1:p.Thr197=
XM_011537477.1:c.898A=	XP_011535779.1:p.Thr300=
XM_006719963.3:c.733A=	XP_006720026.2:p.Thr245=
XM_011537474.2:c.982A=	XP_011535776.2:p.Thr328=
XM_011537475.2:c.796A=	XP_011535777.2:p.Thr266=
XM_011537476.2:c.589A=	XP_011535778.1:p.Thr197=
NM_019616.4:c.829A= MANE Select	NP_062562.1:p.Thr277=
NR_051961.2:n.913A=
NM_001267554.2:c.643A=	NP_001254483.1:p.Thr215=