Canonical Allele Identifier: CA2120135662

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113932T= , CM000675.2:g.113113932T=	GRCh38
NC_000013.10:g.113768246T= , CM000675.1:g.113768246T=	GRCh37
NC_000013.9:g.112816247T=	NCBI36
NG_009262.1:g.13142T= , LRG_554:g.13142T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.336T= MANE Select	ENSP00000329546.4:p.Pro112=
ENST00000346342.7:c.336T=	ENSP00000329546.3:p.Pro112=
ENST00000375581.3:c.402T=	ENSP00000364731.3:p.Pro134=
ENST00000444337.1:c.*144T=	ENSP00000387669.1:n.*144T=
ENST00000473085.1:n.283T=
ENST00000479674.1:n.669T=
ENST00000541084.5:c.150T=	ENSP00000442051.2:p.Pro50=
NM_000131.4:c.402T= , LRG_554t1:c.402T=	NP_000122.1:p.Pro134=
NM_001267554.1:c.150T=	NP_001254483.1:p.Pro50=
NM_019616.3:c.336T= , LRG_554t2:c.336T=	NP_062562.1:p.Pro112=
NR_051961.1:n.423T=
XM_006719963.2:c.336T=	XP_006720026.1:p.Pro112=
XM_011537474.1:c.336T=	XP_011535776.1:p.Pro112=
XM_011537475.1:c.150T=	XP_011535777.1:p.Pro50=
XM_011537477.1:c.297T=	XP_011535779.1:p.Pro99=
XM_006719963.3:c.381T=	XP_006720026.2:p.Pro127=
XM_011537474.2:c.381T=	XP_011535776.2:p.Pro127=
XM_011537475.2:c.195T=	XP_011535777.2:p.Pro65=
NM_019616.4:c.336T= MANE Select	NP_062562.1:p.Pro112=
NR_051961.2:n.420T=
NM_001267554.2:c.150T=	NP_001254483.1:p.Pro50=