Canonical Allele Identifier: CA2120142399

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118683T= , CM000675.2:g.113118683T=	GRCh38
NC_000013.10:g.113772997T= , CM000675.1:g.113772997T=	GRCh37
NC_000013.9:g.112820998T=	NCBI36
NG_009258.1:g.885T= , LRG_548:g.885T=
NG_009262.1:g.17893T= , LRG_554:g.17893T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1010T= MANE Select	ENSP00000329546.4:p.Val337=
ENST00000346342.7:c.1010T=	ENSP00000329546.3:p.Val337=
ENST00000375581.3:c.1076T=	ENSP00000364731.3:p.Val359=
ENST00000541084.5:c.824T=	ENSP00000442051.2:p.Val275=
NM_000131.4:c.1076T= , LRG_554t1:c.1076T=	NP_000122.1:p.Val359=
NM_001267554.1:c.824T=	NP_001254483.1:p.Val275=
NM_019616.3:c.1010T= , LRG_554t2:c.1010T=	NP_062562.1:p.Val337=
NR_051961.1:n.1097T=
XM_006719963.2:c.869T=	XP_006720026.1:p.Val290=
XM_011537474.1:c.1118T=	XP_011535776.1:p.Val373=
XM_011537475.1:c.932T=	XP_011535777.1:p.Val311=
XM_011537476.1:c.770T=	XP_011535778.1:p.Val257=
XM_011537477.1:c.1079T=	XP_011535779.1:p.Val360=
XM_006719963.3:c.914T=	XP_006720026.2:p.Val305=
XM_011537474.2:c.1163T=	XP_011535776.2:p.Val388=
XM_011537475.2:c.977T=	XP_011535777.2:p.Val326=
XM_011537476.2:c.770T=	XP_011535778.1:p.Val257=
NM_019616.4:c.1010T= MANE Select	NP_062562.1:p.Val337=
NR_051961.2:n.1094T=
NM_001267554.2:c.824T=	NP_001254483.1:p.Val275=