Canonical Allele Identifier: CA2120142140

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118602C= , CM000675.2:g.113118602C=	GRCh38
NC_000013.10:g.113772916C= , CM000675.1:g.113772916C=	GRCh37
NC_000013.9:g.112820917C=	NCBI36
NG_009258.1:g.804C= , LRG_548:g.804C=
NG_009262.1:g.17812C= , LRG_554:g.17812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.929C= MANE Select	ENSP00000329546.4:p.Thr310=
ENST00000346342.7:c.929C=	ENSP00000329546.3:p.Thr310=
ENST00000375581.3:c.995C=	ENSP00000364731.3:p.Thr332=
ENST00000541084.5:c.743C=	ENSP00000442051.2:p.Thr248=
NM_000131.4:c.995C= , LRG_554t1:c.995C=	NP_000122.1:p.Thr332=
NM_001267554.1:c.743C=	NP_001254483.1:p.Thr248=
NM_019616.3:c.929C= , LRG_554t2:c.929C=	NP_062562.1:p.Thr310=
NR_051961.1:n.1016C=
XM_006719963.2:c.788C=	XP_006720026.1:p.Thr263=
XM_011537474.1:c.1037C=	XP_011535776.1:p.Thr346=
XM_011537475.1:c.851C=	XP_011535777.1:p.Thr284=
XM_011537476.1:c.689C=	XP_011535778.1:p.Thr230=
XM_011537477.1:c.998C=	XP_011535779.1:p.Thr333=
XM_006719963.3:c.833C=	XP_006720026.2:p.Thr278=
XM_011537474.2:c.1082C=	XP_011535776.2:p.Thr361=
XM_011537475.2:c.896C=	XP_011535777.2:p.Thr299=
XM_011537476.2:c.689C=	XP_011535778.1:p.Thr230=
NM_019616.4:c.929C= MANE Select	NP_062562.1:p.Thr310=
NR_051961.2:n.1013C=
NM_001267554.2:c.743C=	NP_001254483.1:p.Thr248=