Canonical Allele Identifier: CA2120142723

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118819T= , CM000675.2:g.113118819T=	GRCh38
NC_000013.10:g.113773133T= , CM000675.1:g.113773133T=	GRCh37
NC_000013.9:g.112821134T=	NCBI36
NG_009258.1:g.1021T= , LRG_548:g.1021T=
NG_009262.1:g.18029T= , LRG_554:g.18029T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1146T= MANE Select	ENSP00000329546.4:p.Ser382=
ENST00000346342.7:c.1146T=	ENSP00000329546.3:p.Ser382=
ENST00000375581.3:c.1212T=	ENSP00000364731.3:p.Ser404=
ENST00000541084.5:c.960T=	ENSP00000442051.2:p.Ser320=
NM_000131.4:c.1212T= , LRG_554t1:c.1212T=	NP_000122.1:p.Ser404=
NM_001267554.1:c.960T=	NP_001254483.1:p.Ser320=
NM_019616.3:c.1146T= , LRG_554t2:c.1146T=	NP_062562.1:p.Ser382=
NR_051961.1:n.1233T=
XM_006719963.2:c.1005T=	XP_006720026.1:p.Ser335=
XM_011537474.1:c.1254T=	XP_011535776.1:p.Ser418=
XM_011537475.1:c.1068T=	XP_011535777.1:p.Ser356=
XM_011537476.1:c.906T=	XP_011535778.1:p.Ser302=
XM_011537477.1:c.1215T=	XP_011535779.1:p.Ser405=
XM_006719963.3:c.1050T=	XP_006720026.2:p.Ser350=
XM_011537474.2:c.1299T=	XP_011535776.2:p.Ser433=
XM_011537475.2:c.1113T=	XP_011535777.2:p.Ser371=
XM_011537476.2:c.906T=	XP_011535778.1:p.Ser302=
NM_019616.4:c.1146T= MANE Select	NP_062562.1:p.Ser382=
NR_051961.2:n.1230T=
NM_001267554.2:c.960T=	NP_001254483.1:p.Ser320=