Canonical Allele Identifier: CA2120141423

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118272T= , CM000675.2:g.113118272T=	GRCh38
NC_000013.10:g.113772586T= , CM000675.1:g.113772586T=	GRCh37
NC_000013.9:g.112820587T=	NCBI36
NG_009258.1:g.474T= , LRG_548:g.474T=
NG_009262.1:g.17482T= , LRG_554:g.17482T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.740-141T= MANE Select	ENSP00000329546.4:n.740-141T=
ENST00000346342.7:c.740-141T=	ENSP00000329546.3:n.740-141T=
ENST00000375581.3:c.806-141T=	ENSP00000364731.3:n.806-141T=
ENST00000541084.5:c.554-141T=	ENSP00000442051.2:n.554-141T=
NM_000131.4:c.806-141T= , LRG_554t1:c.806-141T=	NP_000122.1:n.806-141T=
NM_001267554.1:c.554-141T=	NP_001254483.1:n.554-141T=
NM_019616.3:c.740-141T= , LRG_554t2:c.740-141T=	NP_062562.1:n.740-141T=
NR_051961.1:n.827-141T=
XM_006719963.2:c.599-141T=	XP_006720026.1:n.599-141T=
XM_011537474.1:c.848-141T=	XP_011535776.1:n.848-141T=
XM_011537475.1:c.662-141T=	XP_011535777.1:n.662-141T=
XM_011537476.1:c.500-141T=	XP_011535778.1:n.500-141T=
XM_011537477.1:c.809-141T=	XP_011535779.1:n.809-141T=
XM_006719963.3:c.644-141T=	XP_006720026.2:n.644-141T=
XM_011537474.2:c.893-141T=	XP_011535776.2:n.893-141T=
XM_011537475.2:c.707-141T=	XP_011535777.2:n.707-141T=
XM_011537476.2:c.500-141T=	XP_011535778.1:n.500-141T=
NM_019616.4:c.740-141T= MANE Select	NP_062562.1:n.740-141T=
NR_051961.2:n.824-141T=
NM_001267554.2:c.554-141T=	NP_001254483.1:n.554-141T=