Canonical Allele Identifier: CA2120142565

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118733A= , CM000675.2:g.113118733A=	GRCh38
NC_000013.10:g.113773047A= , CM000675.1:g.113773047A=	GRCh37
NC_000013.9:g.112821048A=	NCBI36
NG_009258.1:g.935A= , LRG_548:g.935A=
NG_009262.1:g.17943A= , LRG_554:g.17943A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1060A= MANE Select	ENSP00000329546.4:p.Lys354=
ENST00000346342.7:c.1060A=	ENSP00000329546.3:p.Lys354=
ENST00000375581.3:c.1126A=	ENSP00000364731.3:p.Lys376=
ENST00000541084.5:c.874A=	ENSP00000442051.2:p.Lys292=
NM_000131.4:c.1126A= , LRG_554t1:c.1126A=	NP_000122.1:p.Lys376=
NM_001267554.1:c.874A=	NP_001254483.1:p.Lys292=
NM_019616.3:c.1060A= , LRG_554t2:c.1060A=	NP_062562.1:p.Lys354=
NR_051961.1:n.1147A=
XM_006719963.2:c.919A=	XP_006720026.1:p.Lys307=
XM_011537474.1:c.1168A=	XP_011535776.1:p.Lys390=
XM_011537475.1:c.982A=	XP_011535777.1:p.Lys328=
XM_011537476.1:c.820A=	XP_011535778.1:p.Lys274=
XM_011537477.1:c.1129A=	XP_011535779.1:p.Lys377=
XM_006719963.3:c.964A=	XP_006720026.2:p.Lys322=
XM_011537474.2:c.1213A=	XP_011535776.2:p.Lys405=
XM_011537475.2:c.1027A=	XP_011535777.2:p.Lys343=
XM_011537476.2:c.820A=	XP_011535778.1:p.Lys274=
NM_019616.4:c.1060A= MANE Select	NP_062562.1:p.Lys354=
NR_051961.2:n.1144A=
NM_001267554.2:c.874A=	NP_001254483.1:p.Lys292=