Canonical Allele Identifier: CA2120135615

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113912T= , CM000675.2:g.113113912T=	GRCh38
NC_000013.10:g.113768226T= , CM000675.1:g.113768226T=	GRCh37
NC_000013.9:g.112816227T=	NCBI36
NG_009262.1:g.13122T= , LRG_554:g.13122T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.316T= MANE Select	ENSP00000329546.4:p.Tyr106=
ENST00000346342.7:c.316T=	ENSP00000329546.3:p.Tyr106=
ENST00000375581.3:c.382T=	ENSP00000364731.3:p.Tyr128=
ENST00000444337.1:c.*124T=	ENSP00000387669.1:n.*124T=
ENST00000473085.1:n.263T=
ENST00000479674.1:n.649T=
ENST00000541084.5:c.130T=	ENSP00000442051.2:p.Tyr44=
NM_000131.4:c.382T= , LRG_554t1:c.382T=	NP_000122.1:p.Tyr128=
NM_001267554.1:c.130T=	NP_001254483.1:p.Tyr44=
NM_019616.3:c.316T= , LRG_554t2:c.316T=	NP_062562.1:p.Tyr106=
NR_051961.1:n.403T=
XM_006719963.2:c.316T=	XP_006720026.1:p.Tyr106=
XM_011537474.1:c.316T=	XP_011535776.1:p.Tyr106=
XM_011537475.1:c.130T=	XP_011535777.1:p.Tyr44=
XM_011537477.1:c.277T=	XP_011535779.1:p.Tyr93=
XM_006719963.3:c.361T=	XP_006720026.2:p.Tyr121=
XM_011537474.2:c.361T=	XP_011535776.2:p.Tyr121=
XM_011537475.2:c.175T=	XP_011535777.2:p.Tyr59=
NM_019616.4:c.316T= MANE Select	NP_062562.1:p.Tyr106=
NR_051961.2:n.400T=
NM_001267554.2:c.130T=	NP_001254483.1:p.Tyr44=