Canonical Allele Identifier: CA2120142375

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118669C= , CM000675.2:g.113118669C=	GRCh38
NC_000013.10:g.113772983C= , CM000675.1:g.113772983C=	GRCh37
NC_000013.9:g.112820984C=	NCBI36
NG_009258.1:g.871C= , LRG_548:g.871C=
NG_009262.1:g.17879C= , LRG_554:g.17879C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.996C= MANE Select	ENSP00000329546.4:p.Ala332=
ENST00000346342.7:c.996C=	ENSP00000329546.3:p.Ala332=
ENST00000375581.3:c.1062C=	ENSP00000364731.3:p.Ala354=
ENST00000541084.5:c.810C=	ENSP00000442051.2:p.Ala270=
NM_000131.4:c.1062C= , LRG_554t1:c.1062C=	NP_000122.1:p.Ala354=
NM_001267554.1:c.810C=	NP_001254483.1:p.Ala270=
NM_019616.3:c.996C= , LRG_554t2:c.996C=	NP_062562.1:p.Ala332=
NR_051961.1:n.1083C=
XM_006719963.2:c.855C=	XP_006720026.1:p.Ala285=
XM_011537474.1:c.1104C=	XP_011535776.1:p.Ala368=
XM_011537475.1:c.918C=	XP_011535777.1:p.Ala306=
XM_011537476.1:c.756C=	XP_011535778.1:p.Ala252=
XM_011537477.1:c.1065C=	XP_011535779.1:p.Ala355=
XM_006719963.3:c.900C=	XP_006720026.2:p.Ala300=
XM_011537474.2:c.1149C=	XP_011535776.2:p.Ala383=
XM_011537475.2:c.963C=	XP_011535777.2:p.Ala321=
XM_011537476.2:c.756C=	XP_011535778.1:p.Ala252=
NM_019616.4:c.996C= MANE Select	NP_062562.1:p.Ala332=
NR_051961.2:n.1080C=
NM_001267554.2:c.810C=	NP_001254483.1:p.Ala270=