Canonical Allele Identifier: CA2120135719

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113958C= , CM000675.2:g.113113958C=	GRCh38
NC_000013.10:g.113768272C= , CM000675.1:g.113768272C=	GRCh37
NC_000013.9:g.112816273C=	NCBI36
NG_009262.1:g.13168C= , LRG_554:g.13168C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.362C= MANE Select	ENSP00000329546.4:p.Thr121=
ENST00000346342.7:c.362C=	ENSP00000329546.3:p.Thr121=
ENST00000375581.3:c.428C=	ENSP00000364731.3:p.Thr143=
ENST00000444337.1:c.*170C=	ENSP00000387669.1:n.*170C=
ENST00000473085.1:n.309C=
ENST00000479674.1:n.695C=
ENST00000541084.5:c.176C=	ENSP00000442051.2:p.Thr59=
NM_000131.4:c.428C= , LRG_554t1:c.428C=	NP_000122.1:p.Thr143=
NM_001267554.1:c.176C=	NP_001254483.1:p.Thr59=
NM_019616.3:c.362C= , LRG_554t2:c.362C=	NP_062562.1:p.Thr121=
NR_051961.1:n.449C=
XM_006719963.2:c.362C=	XP_006720026.1:p.Thr121=
XM_011537474.1:c.362C=	XP_011535776.1:p.Thr121=
XM_011537475.1:c.176C=	XP_011535777.1:p.Thr59=
XM_011537477.1:c.323C=	XP_011535779.1:p.Thr108=
XM_006719963.3:c.407C=	XP_006720026.2:p.Thr136=
XM_011537474.2:c.407C=	XP_011535776.2:p.Thr136=
XM_011537475.2:c.221C=	XP_011535777.2:p.Thr74=
NM_019616.4:c.362C= MANE Select	NP_062562.1:p.Thr121=
NR_051961.2:n.446C=
NM_001267554.2:c.176C=	NP_001254483.1:p.Thr59=