Canonical Allele Identifier: CA2120141986

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118516C= , CM000675.2:g.113118516C=	GRCh38
NC_000013.10:g.113772830C= , CM000675.1:g.113772830C=	GRCh37
NC_000013.9:g.112820831C=	NCBI36
NG_009258.1:g.718C= , LRG_548:g.718C=
NG_009262.1:g.17726C= , LRG_554:g.17726C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.843C= MANE Select	ENSP00000329546.4:p.Ile281=
ENST00000346342.7:c.843C=	ENSP00000329546.3:p.Ile281=
ENST00000375581.3:c.909C=	ENSP00000364731.3:p.Ile303=
ENST00000541084.5:c.657C=	ENSP00000442051.2:p.Ile219=
NM_000131.4:c.909C= , LRG_554t1:c.909C=	NP_000122.1:p.Ile303=
NM_001267554.1:c.657C=	NP_001254483.1:p.Ile219=
NM_019616.3:c.843C= , LRG_554t2:c.843C=	NP_062562.1:p.Ile281=
NR_051961.1:n.930C=
XM_006719963.2:c.702C=	XP_006720026.1:p.Ile234=
XM_011537474.1:c.951C=	XP_011535776.1:p.Ile317=
XM_011537475.1:c.765C=	XP_011535777.1:p.Ile255=
XM_011537476.1:c.603C=	XP_011535778.1:p.Ile201=
XM_011537477.1:c.912C=	XP_011535779.1:p.Ile304=
XM_006719963.3:c.747C=	XP_006720026.2:p.Ile249=
XM_011537474.2:c.996C=	XP_011535776.2:p.Ile332=
XM_011537475.2:c.810C=	XP_011535777.2:p.Ile270=
XM_011537476.2:c.603C=	XP_011535778.1:p.Ile201=
NM_019616.4:c.843C= MANE Select	NP_062562.1:p.Ile281=
NR_051961.2:n.927C=
NM_001267554.2:c.657C=	NP_001254483.1:p.Ile219=