Canonical Allele Identifier: CA2120135733

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113960C= , CM000675.2:g.113113960C=	GRCh38
NC_000013.10:g.113768274C= , CM000675.1:g.113768274C=	GRCh37
NC_000013.9:g.112816275C=	NCBI36
NG_009262.1:g.13170C= , LRG_554:g.13170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364C= MANE Select	ENSP00000329546.4:p.His122=
ENST00000346342.7:c.364C=	ENSP00000329546.3:p.His122=
ENST00000375581.3:c.430C=	ENSP00000364731.3:p.His144=
ENST00000444337.1:c.*172C=	ENSP00000387669.1:n.*172C=
ENST00000473085.1:n.311C=
ENST00000479674.1:n.697C=
ENST00000541084.5:c.178C=	ENSP00000442051.2:p.His60=
NM_000131.4:c.430C= , LRG_554t1:c.430C=	NP_000122.1:p.His144=
NM_001267554.1:c.178C=	NP_001254483.1:p.His60=
NM_019616.3:c.364C= , LRG_554t2:c.364C=	NP_062562.1:p.His122=
NR_051961.1:n.451C=
XM_006719963.2:c.364C=	XP_006720026.1:p.Leu122=
XM_011537474.1:c.364C=	XP_011535776.1:p.Gln122=
XM_011537475.1:c.178C=	XP_011535777.1:p.Gln60=
XM_011537477.1:c.325C=	XP_011535779.1:p.Gln109=
XM_006719963.3:c.409C=	XP_006720026.2:p.Leu137=
XM_011537474.2:c.409C=	XP_011535776.2:p.Gln137=
XM_011537475.2:c.223C=	XP_011535777.2:p.Gln75=
NM_019616.4:c.364C= MANE Select	NP_062562.1:p.His122=
NR_051961.2:n.448C=
NM_001267554.2:c.178C=	NP_001254483.1:p.His60=