Canonical Allele Identifier: CA2120143060

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118973C= , CM000675.2:g.113118973C=	GRCh38
NC_000013.10:g.113773287C= , CM000675.1:g.113773287C=	GRCh37
NC_000013.9:g.112821288C=	NCBI36
NG_009258.1:g.1175C= , LRG_548:g.1175C=
NG_009262.1:g.18183C= , LRG_554:g.18183C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1300C= MANE Select	ENSP00000329546.4:p.Arg434=
ENST00000346342.7:c.1300C=	ENSP00000329546.3:p.Arg434=
ENST00000375581.3:c.1366C=	ENSP00000364731.3:p.Arg456=
ENST00000541084.5:c.1114C=	ENSP00000442051.2:p.Arg372=
NM_000131.4:c.1366C= , LRG_554t1:c.1366C=	NP_000122.1:p.Arg456=
NM_001267554.1:c.1114C=	NP_001254483.1:p.Arg372=
NM_019616.3:c.1300C= , LRG_554t2:c.1300C=	NP_062562.1:p.Arg434=
NR_051961.1:n.1387C=
XM_006719963.2:c.1159C=	XP_006720026.1:p.Arg387=
XM_011537474.1:c.1408C=	XP_011535776.1:p.Arg470=
XM_011537475.1:c.1222C=	XP_011535777.1:p.Arg408=
XM_011537476.1:c.1060C=	XP_011535778.1:p.Arg354=
XM_011537477.1:c.1369C=	XP_011535779.1:p.Arg457=
XM_006719963.3:c.1204C=	XP_006720026.2:p.Arg402=
XM_011537474.2:c.1453C=	XP_011535776.2:p.Arg485=
XM_011537475.2:c.1267C=	XP_011535777.2:p.Arg423=
XM_011537476.2:c.1060C=	XP_011535778.1:p.Arg354=
NM_019616.4:c.1300C= MANE Select	NP_062562.1:p.Arg434=
NR_051961.2:n.1384C=
NM_001267554.2:c.1114C=	NP_001254483.1:p.Arg372=