Canonical Allele Identifier: CA2120141984

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118515T= , CM000675.2:g.113118515T=	GRCh38
NC_000013.10:g.113772829T= , CM000675.1:g.113772829T=	GRCh37
NC_000013.9:g.112820830T=	NCBI36
NG_009258.1:g.717T= , LRG_548:g.717T=
NG_009262.1:g.17725T= , LRG_554:g.17725T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.842T= MANE Select	ENSP00000329546.4:p.Ile281=
ENST00000346342.7:c.842T=	ENSP00000329546.3:p.Ile281=
ENST00000375581.3:c.908T=	ENSP00000364731.3:p.Ile303=
ENST00000541084.5:c.656T=	ENSP00000442051.2:p.Ile219=
NM_000131.4:c.908T= , LRG_554t1:c.908T=	NP_000122.1:p.Ile303=
NM_001267554.1:c.656T=	NP_001254483.1:p.Ile219=
NM_019616.3:c.842T= , LRG_554t2:c.842T=	NP_062562.1:p.Ile281=
NR_051961.1:n.929T=
XM_006719963.2:c.701T=	XP_006720026.1:p.Ile234=
XM_011537474.1:c.950T=	XP_011535776.1:p.Ile317=
XM_011537475.1:c.764T=	XP_011535777.1:p.Ile255=
XM_011537476.1:c.602T=	XP_011535778.1:p.Ile201=
XM_011537477.1:c.911T=	XP_011535779.1:p.Ile304=
XM_006719963.3:c.746T=	XP_006720026.2:p.Ile249=
XM_011537474.2:c.995T=	XP_011535776.2:p.Ile332=
XM_011537475.2:c.809T=	XP_011535777.2:p.Ile270=
XM_011537476.2:c.602T=	XP_011535778.1:p.Ile201=
NM_019616.4:c.842T= MANE Select	NP_062562.1:p.Ile281=
NR_051961.2:n.926T=
NM_001267554.2:c.656T=	NP_001254483.1:p.Ile219=