Canonical Allele Identifier: CA2120144014

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119512C= , CM000675.2:g.113119512C=	GRCh38
NC_000013.10:g.113773826C= , CM000675.1:g.113773826C=	GRCh37
NC_000013.9:g.112821827C=	NCBI36
NG_009258.1:g.1714C= , LRG_548:g.1714C=
NG_009262.1:g.18722C= , LRG_554:g.18722C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*504C= MANE Select	ENSP00000329546.4:n.*504C=
ENST00000346342.7:c.*504C=	ENSP00000329546.3:n.*504C=
ENST00000375581.3:c.*504C=	ENSP00000364731.3:n.*504C=
ENST00000541084.5:c.*504C=	ENSP00000442051.2:n.*504C=
NM_000131.4:c.*504C= , LRG_554t1:c.*504C=	NP_000122.1:n.*504C=
NM_001267554.1:c.*504C=	NP_001254483.1:n.*504C=
NM_019616.3:c.*504C= , LRG_554t2:c.*504C=	NP_062562.1:n.*504C=
NR_051961.1:n.1926C=
XM_006719963.2:c.*504C=	XP_006720026.1:n.*504C=
XM_011537474.1:c.*504C=	XP_011535776.1:n.*504C=
XM_011537475.1:c.*504C=	XP_011535777.1:n.*504C=
XM_011537476.1:c.*504C=	XP_011535778.1:n.*504C=
XM_011537477.1:c.*504C=	XP_011535779.1:n.*504C=
XM_006719963.3:c.*504C=	XP_006720026.2:n.*504C=
XM_011537474.2:c.*504C=	XP_011535776.2:n.*504C=
XM_011537475.2:c.*504C=	XP_011535777.2:n.*504C=
XM_011537476.2:c.*504C=	XP_011535778.1:n.*504C=
NM_019616.4:c.*504C= MANE Select	NP_062562.1:n.*504C=
NR_051961.2:n.1923C=
NM_001267554.2:c.*504C=	NP_001254483.1:n.*504C=