Canonical Allele Identifier: CA2120144830

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119862C= , CM000675.2:g.113119862C=	GRCh38
NC_000013.10:g.113774176C= , CM000675.1:g.113774176C=	GRCh37
NC_000013.9:g.112822177C=	NCBI36
NG_009258.1:g.2064C= , LRG_548:g.2064C=
NG_009262.1:g.19072C= , LRG_554:g.19072C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*854C= MANE Select	ENSP00000329546.4:n.*854C=
ENST00000346342.7:c.*854C=	ENSP00000329546.3:n.*854C=
ENST00000375581.3:c.*854C=	ENSP00000364731.3:n.*854C=
ENST00000541084.5:c.*854C=	ENSP00000442051.2:n.*854C=
NM_000131.4:c.*854C= , LRG_554t1:c.*854C=	NP_000122.1:n.*854C=
NM_001267554.1:c.*854C=	NP_001254483.1:n.*854C=
NM_019616.3:c.*854C= , LRG_554t2:c.*854C=	NP_062562.1:n.*854C=
NR_051961.1:n.2276C=
XM_006719963.2:c.*854C=	XP_006720026.1:n.*854C=
XM_011537474.1:c.*854C=	XP_011535776.1:n.*854C=
XM_011537475.1:c.*854C=	XP_011535777.1:n.*854C=
XM_011537476.1:c.*854C=	XP_011535778.1:n.*854C=
XM_011537477.1:c.*854C=	XP_011535779.1:n.*854C=
XM_006719963.3:c.*854C=	XP_006720026.2:n.*854C=
XM_011537474.2:c.*854C=	XP_011535776.2:n.*854C=
XM_011537475.2:c.*854C=	XP_011535777.2:n.*854C=
XM_011537476.2:c.*854C=	XP_011535778.1:n.*854C=
NM_019616.4:c.*854C= MANE Select	NP_062562.1:n.*854C=
NR_051961.2:n.2273C=
NM_001267554.2:c.*854C=	NP_001254483.1:n.*854C=