Canonical Allele Identifier: CA2120142312

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118660C= , CM000675.2:g.113118660C=	GRCh38
NC_000013.10:g.113772974C= , CM000675.1:g.113772974C=	GRCh37
NC_000013.9:g.112820975C=	NCBI36
NG_009258.1:g.862C= , LRG_548:g.862C=
NG_009262.1:g.17870C= , LRG_554:g.17870C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.987C= MANE Select	ENSP00000329546.4:p.Gly329=
ENST00000346342.7:c.987C=	ENSP00000329546.3:p.Gly329=
ENST00000375581.3:c.1053C=	ENSP00000364731.3:p.Gly351=
ENST00000541084.5:c.801C=	ENSP00000442051.2:p.Gly267=
NM_000131.4:c.1053C= , LRG_554t1:c.1053C=	NP_000122.1:p.Gly351=
NM_001267554.1:c.801C=	NP_001254483.1:p.Gly267=
NM_019616.3:c.987C= , LRG_554t2:c.987C=	NP_062562.1:p.Gly329=
NR_051961.1:n.1074C=
XM_006719963.2:c.846C=	XP_006720026.1:p.Gly282=
XM_011537474.1:c.1095C=	XP_011535776.1:p.Gly365=
XM_011537475.1:c.909C=	XP_011535777.1:p.Gly303=
XM_011537476.1:c.747C=	XP_011535778.1:p.Gly249=
XM_011537477.1:c.1056C=	XP_011535779.1:p.Gly352=
XM_006719963.3:c.891C=	XP_006720026.2:p.Gly297=
XM_011537474.2:c.1140C=	XP_011535776.2:p.Gly380=
XM_011537475.2:c.954C=	XP_011535777.2:p.Gly318=
XM_011537476.2:c.747C=	XP_011535778.1:p.Gly249=
NM_019616.4:c.987C= MANE Select	NP_062562.1:p.Gly329=
NR_051961.2:n.1071C=
NM_001267554.2:c.801C=	NP_001254483.1:p.Gly267=