Canonical Allele Identifier: CA2120142657

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118770T= , CM000675.2:g.113118770T=	GRCh38
NC_000013.10:g.113773084T= , CM000675.1:g.113773084T=	GRCh37
NC_000013.9:g.112821085T=	NCBI36
NG_009258.1:g.972T= , LRG_548:g.972T=
NG_009262.1:g.17980T= , LRG_554:g.17980T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1097T= MANE Select	ENSP00000329546.4:p.Phe366=
ENST00000346342.7:c.1097T=	ENSP00000329546.3:p.Phe366=
ENST00000375581.3:c.1163T=	ENSP00000364731.3:p.Phe388=
ENST00000541084.5:c.911T=	ENSP00000442051.2:p.Phe304=
NM_000131.4:c.1163T= , LRG_554t1:c.1163T=	NP_000122.1:p.Phe388=
NM_001267554.1:c.911T=	NP_001254483.1:p.Phe304=
NM_019616.3:c.1097T= , LRG_554t2:c.1097T=	NP_062562.1:p.Phe366=
NR_051961.1:n.1184T=
XM_006719963.2:c.956T=	XP_006720026.1:p.Phe319=
XM_011537474.1:c.1205T=	XP_011535776.1:p.Phe402=
XM_011537475.1:c.1019T=	XP_011535777.1:p.Phe340=
XM_011537476.1:c.857T=	XP_011535778.1:p.Phe286=
XM_011537477.1:c.1166T=	XP_011535779.1:p.Phe389=
XM_006719963.3:c.1001T=	XP_006720026.2:p.Phe334=
XM_011537474.2:c.1250T=	XP_011535776.2:p.Phe417=
XM_011537475.2:c.1064T=	XP_011535777.2:p.Phe355=
XM_011537476.2:c.857T=	XP_011535778.1:p.Phe286=
NM_019616.4:c.1097T= MANE Select	NP_062562.1:p.Phe366=
NR_051961.2:n.1181T=
NM_001267554.2:c.911T=	NP_001254483.1:p.Phe304=