Canonical Allele Identifier: CA2018007885

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118777C= , CM000675.2:g.113118777C=	GRCh38
NC_000013.10:g.113773091C= , CM000675.1:g.113773091C=	GRCh37
NC_000013.9:g.112821092C=	NCBI36
NG_009258.1:g.979C= , LRG_548:g.979C=
NG_009262.1:g.17987C= , LRG_554:g.17987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1104C= MANE Select	ENSP00000329546.4:p.Ala368=
ENST00000346342.7:c.1104C=	ENSP00000329546.3:p.Ala368=
ENST00000375581.3:c.1170C=	ENSP00000364731.3:p.Ala390=
ENST00000541084.5:c.918C=	ENSP00000442051.2:p.Ala306=
NM_000131.4:c.1170C= , LRG_554t1:c.1170C=	NP_000122.1:p.Ala390=
NM_001267554.1:c.918C=	NP_001254483.1:p.Ala306=
NM_019616.3:c.1104C= , LRG_554t2:c.1104C=	NP_062562.1:p.Ala368=
NR_051961.1:n.1191C=
XM_006719963.2:c.963C=	XP_006720026.1:p.Ala321=
XM_011537474.1:c.1212C=	XP_011535776.1:p.Ala404=
XM_011537475.1:c.1026C=	XP_011535777.1:p.Ala342=
XM_011537476.1:c.864C=	XP_011535778.1:p.Ala288=
XM_011537477.1:c.1173C=	XP_011535779.1:p.Ala391=
XM_006719963.3:c.1008C=	XP_006720026.2:p.Ala336=
XM_011537474.2:c.1257C=	XP_011535776.2:p.Ala419=
XM_011537475.2:c.1071C=	XP_011535777.2:p.Ala357=
XM_011537476.2:c.864C=	XP_011535778.1:p.Ala288=
NM_019616.4:c.1104C= MANE Select	NP_062562.1:p.Ala368=
NR_051961.2:n.1188C=
NM_001267554.2:c.918C=	NP_001254483.1:p.Ala306=