Canonical Allele Identifier: CA2120142521

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118721C= , CM000675.2:g.113118721C=	GRCh38
NC_000013.10:g.113773035C= , CM000675.1:g.113773035C=	GRCh37
NC_000013.9:g.112821036C=	NCBI36
NG_009258.1:g.923C= , LRG_548:g.923C=
NG_009262.1:g.17931C= , LRG_554:g.17931C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1048C= MANE Select	ENSP00000329546.4:p.Gln350=
ENST00000346342.7:c.1048C=	ENSP00000329546.3:p.Gln350=
ENST00000375581.3:c.1114C=	ENSP00000364731.3:p.Gln372=
ENST00000541084.5:c.862C=	ENSP00000442051.2:p.Gln288=
NM_000131.4:c.1114C= , LRG_554t1:c.1114C=	NP_000122.1:p.Gln372=
NM_001267554.1:c.862C=	NP_001254483.1:p.Gln288=
NM_019616.3:c.1048C= , LRG_554t2:c.1048C=	NP_062562.1:p.Gln350=
NR_051961.1:n.1135C=
XM_006719963.2:c.907C=	XP_006720026.1:p.Gln303=
XM_011537474.1:c.1156C=	XP_011535776.1:p.Gln386=
XM_011537475.1:c.970C=	XP_011535777.1:p.Gln324=
XM_011537476.1:c.808C=	XP_011535778.1:p.Gln270=
XM_011537477.1:c.1117C=	XP_011535779.1:p.Gln373=
XM_006719963.3:c.952C=	XP_006720026.2:p.Gln318=
XM_011537474.2:c.1201C=	XP_011535776.2:p.Gln401=
XM_011537475.2:c.1015C=	XP_011535777.2:p.Gln339=
XM_011537476.2:c.808C=	XP_011535778.1:p.Gln270=
NM_019616.4:c.1048C= MANE Select	NP_062562.1:p.Gln350=
NR_051961.2:n.1132C=
NM_001267554.2:c.862C=	NP_001254483.1:p.Gln288=