Canonical Allele Identifier: CA2120142200

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118618C= , CM000675.2:g.113118618C=	GRCh38
NC_000013.10:g.113772932C= , CM000675.1:g.113772932C=	GRCh37
NC_000013.9:g.112820933C=	NCBI36
NG_009258.1:g.820C= , LRG_548:g.820C=
NG_009262.1:g.17828C= , LRG_554:g.17828C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.945C= MANE Select	ENSP00000329546.4:p.Arg315=
ENST00000346342.7:c.945C=	ENSP00000329546.3:p.Arg315=
ENST00000375581.3:c.1011C=	ENSP00000364731.3:p.Arg337=
ENST00000541084.5:c.759C=	ENSP00000442051.2:p.Arg253=
NM_000131.4:c.1011C= , LRG_554t1:c.1011C=	NP_000122.1:p.Arg337=
NM_001267554.1:c.759C=	NP_001254483.1:p.Arg253=
NM_019616.3:c.945C= , LRG_554t2:c.945C=	NP_062562.1:p.Arg315=
NR_051961.1:n.1032C=
XM_006719963.2:c.804C=	XP_006720026.1:p.Arg268=
XM_011537474.1:c.1053C=	XP_011535776.1:p.Arg351=
XM_011537475.1:c.867C=	XP_011535777.1:p.Arg289=
XM_011537476.1:c.705C=	XP_011535778.1:p.Arg235=
XM_011537477.1:c.1014C=	XP_011535779.1:p.Arg338=
XM_006719963.3:c.849C=	XP_006720026.2:p.Arg283=
XM_011537474.2:c.1098C=	XP_011535776.2:p.Arg366=
XM_011537475.2:c.912C=	XP_011535777.2:p.Arg304=
XM_011537476.2:c.705C=	XP_011535778.1:p.Arg235=
NM_019616.4:c.945C= MANE Select	NP_062562.1:p.Arg315=
NR_051961.2:n.1029C=
NM_001267554.2:c.759C=	NP_001254483.1:p.Arg253=