Canonical Allele Identifier: CA2120142411

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118689A= , CM000675.2:g.113118689A=	GRCh38
NC_000013.10:g.113773003A= , CM000675.1:g.113773003A=	GRCh37
NC_000013.9:g.112821004A=	NCBI36
NG_009258.1:g.891A= , LRG_548:g.891A=
NG_009262.1:g.17899A= , LRG_554:g.17899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1016A= MANE Select	ENSP00000329546.4:p.Asn339=
ENST00000346342.7:c.1016A=	ENSP00000329546.3:p.Asn339=
ENST00000375581.3:c.1082A=	ENSP00000364731.3:p.Asn361=
ENST00000541084.5:c.830A=	ENSP00000442051.2:p.Asn277=
NM_000131.4:c.1082A= , LRG_554t1:c.1082A=	NP_000122.1:p.Asn361=
NM_001267554.1:c.830A=	NP_001254483.1:p.Asn277=
NM_019616.3:c.1016A= , LRG_554t2:c.1016A=	NP_062562.1:p.Asn339=
NR_051961.1:n.1103A=
XM_006719963.2:c.875A=	XP_006720026.1:p.Asn292=
XM_011537474.1:c.1124A=	XP_011535776.1:p.Asn375=
XM_011537475.1:c.938A=	XP_011535777.1:p.Asn313=
XM_011537476.1:c.776A=	XP_011535778.1:p.Asn259=
XM_011537477.1:c.1085A=	XP_011535779.1:p.Asn362=
XM_006719963.3:c.920A=	XP_006720026.2:p.Asn307=
XM_011537474.2:c.1169A=	XP_011535776.2:p.Asn390=
XM_011537475.2:c.983A=	XP_011535777.2:p.Asn328=
XM_011537476.2:c.776A=	XP_011535778.1:p.Asn259=
NM_019616.4:c.1016A= MANE Select	NP_062562.1:p.Asn339=
NR_051961.2:n.1100A=
NM_001267554.2:c.830A=	NP_001254483.1:p.Asn277=