Canonical Allele Identifier: CA2120142352

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118665C= , CM000675.2:g.113118665C=	GRCh38
NC_000013.10:g.113772979C= , CM000675.1:g.113772979C=	GRCh37
NC_000013.9:g.112820980C=	NCBI36
NG_009258.1:g.867C= , LRG_548:g.867C=
NG_009262.1:g.17875C= , LRG_554:g.17875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.992C= MANE Select	ENSP00000329546.4:p.Thr331=
ENST00000346342.7:c.992C=	ENSP00000329546.3:p.Thr331=
ENST00000375581.3:c.1058C=	ENSP00000364731.3:p.Thr353=
ENST00000541084.5:c.806C=	ENSP00000442051.2:p.Thr269=
NM_000131.4:c.1058C= , LRG_554t1:c.1058C=	NP_000122.1:p.Thr353=
NM_001267554.1:c.806C=	NP_001254483.1:p.Thr269=
NM_019616.3:c.992C= , LRG_554t2:c.992C=	NP_062562.1:p.Thr331=
NR_051961.1:n.1079C=
XM_006719963.2:c.851C=	XP_006720026.1:p.Thr284=
XM_011537474.1:c.1100C=	XP_011535776.1:p.Thr367=
XM_011537475.1:c.914C=	XP_011535777.1:p.Thr305=
XM_011537476.1:c.752C=	XP_011535778.1:p.Thr251=
XM_011537477.1:c.1061C=	XP_011535779.1:p.Thr354=
XM_006719963.3:c.896C=	XP_006720026.2:p.Thr299=
XM_011537474.2:c.1145C=	XP_011535776.2:p.Thr382=
XM_011537475.2:c.959C=	XP_011535777.2:p.Thr320=
XM_011537476.2:c.752C=	XP_011535778.1:p.Thr251=
NM_019616.4:c.992C= MANE Select	NP_062562.1:p.Thr331=
NR_051961.2:n.1076C=
NM_001267554.2:c.806C=	NP_001254483.1:p.Thr269=