Canonical Allele Identifier: CA2120142693

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118786G= , CM000675.2:g.113118786G=	GRCh38
NC_000013.10:g.113773100G= , CM000675.1:g.113773100G=	GRCh37
NC_000013.9:g.112821101G=	NCBI36
NG_009258.1:g.988G= , LRG_548:g.988G=
NG_009262.1:g.17996G= , LRG_554:g.17996G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.1113G= MANE Select	ENSP00000329546.4:p.Ser371=
ENST00000346342.7:c.1113G=	ENSP00000329546.3:p.Ser371=
ENST00000375581.3:c.1179G=	ENSP00000364731.3:p.Ser393=
ENST00000541084.5:c.927G=	ENSP00000442051.2:p.Ser309=
NM_000131.4:c.1179G= , LRG_554t1:c.1179G=	NP_000122.1:p.Ser393=
NM_001267554.1:c.927G=	NP_001254483.1:p.Ser309=
NM_019616.3:c.1113G= , LRG_554t2:c.1113G=	NP_062562.1:p.Ser371=
NR_051961.1:n.1200G=
XM_006719963.2:c.972G=	XP_006720026.1:p.Ser324=
XM_011537474.1:c.1221G=	XP_011535776.1:p.Ser407=
XM_011537475.1:c.1035G=	XP_011535777.1:p.Ser345=
XM_011537476.1:c.873G=	XP_011535778.1:p.Ser291=
XM_011537477.1:c.1182G=	XP_011535779.1:p.Ser394=
XM_006719963.3:c.1017G=	XP_006720026.2:p.Ser339=
XM_011537474.2:c.1266G=	XP_011535776.2:p.Ser422=
XM_011537475.2:c.1080G=	XP_011535777.2:p.Ser360=
XM_011537476.2:c.873G=	XP_011535778.1:p.Ser291=
NM_019616.4:c.1113G= MANE Select	NP_062562.1:p.Ser371=
NR_051961.2:n.1197G=
NM_001267554.2:c.927G=	NP_001254483.1:p.Ser309=