Canonical Allele Identifier: CA2120143552

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119221C= , CM000675.2:g.113119221C=	GRCh38
NC_000013.10:g.113773535C= , CM000675.1:g.113773535C=	GRCh37
NC_000013.9:g.112821536C=	NCBI36
NG_009258.1:g.1423C= , LRG_548:g.1423C=
NG_009262.1:g.18431C= , LRG_554:g.18431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*213C= MANE Select	ENSP00000329546.4:n.*213C=
ENST00000346342.7:c.*213C=	ENSP00000329546.3:n.*213C=
ENST00000375581.3:c.*213C=	ENSP00000364731.3:n.*213C=
ENST00000541084.5:c.*213C=	ENSP00000442051.2:n.*213C=
NM_000131.4:c.*213C= , LRG_554t1:c.*213C=	NP_000122.1:n.*213C=
NM_001267554.1:c.*213C=	NP_001254483.1:n.*213C=
NM_019616.3:c.*213C= , LRG_554t2:c.*213C=	NP_062562.1:n.*213C=
NR_051961.1:n.1635C=
XM_006719963.2:c.*213C=	XP_006720026.1:n.*213C=
XM_011537474.1:c.*213C=	XP_011535776.1:n.*213C=
XM_011537475.1:c.*213C=	XP_011535777.1:n.*213C=
XM_011537476.1:c.*213C=	XP_011535778.1:n.*213C=
XM_011537477.1:c.*213C=	XP_011535779.1:n.*213C=
XM_006719963.3:c.*213C=	XP_006720026.2:n.*213C=
XM_011537474.2:c.*213C=	XP_011535776.2:n.*213C=
XM_011537475.2:c.*213C=	XP_011535777.2:n.*213C=
XM_011537476.2:c.*213C=	XP_011535778.1:n.*213C=
NM_019616.4:c.*213C= MANE Select	NP_062562.1:n.*213C=
NR_051961.2:n.1632C=
NM_001267554.2:c.*213C=	NP_001254483.1:n.*213C=