Canonical Allele Identifier: CA2120142581

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118741A= , CM000675.2:g.113118741A=	GRCh38
NC_000013.10:g.113773055A= , CM000675.1:g.113773055A=	GRCh37
NC_000013.9:g.112821056A=	NCBI36
NG_009258.1:g.943A= , LRG_548:g.943A=
NG_009262.1:g.17951A= , LRG_554:g.17951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1068A= MANE Select	ENSP00000329546.4:p.Gly356=
ENST00000346342.7:c.1068A=	ENSP00000329546.3:p.Gly356=
ENST00000375581.3:c.1134A=	ENSP00000364731.3:p.Gly378=
ENST00000541084.5:c.882A=	ENSP00000442051.2:p.Gly294=
NM_000131.4:c.1134A= , LRG_554t1:c.1134A=	NP_000122.1:p.Gly378=
NM_001267554.1:c.882A=	NP_001254483.1:p.Gly294=
NM_019616.3:c.1068A= , LRG_554t2:c.1068A=	NP_062562.1:p.Gly356=
NR_051961.1:n.1155A=
XM_006719963.2:c.927A=	XP_006720026.1:p.Gly309=
XM_011537474.1:c.1176A=	XP_011535776.1:p.Gly392=
XM_011537475.1:c.990A=	XP_011535777.1:p.Gly330=
XM_011537476.1:c.828A=	XP_011535778.1:p.Gly276=
XM_011537477.1:c.1137A=	XP_011535779.1:p.Gly379=
XM_006719963.3:c.972A=	XP_006720026.2:p.Gly324=
XM_011537474.2:c.1221A=	XP_011535776.2:p.Gly407=
XM_011537475.2:c.1035A=	XP_011535777.2:p.Gly345=
XM_011537476.2:c.828A=	XP_011535778.1:p.Gly276=
NM_019616.4:c.1068A= MANE Select	NP_062562.1:p.Gly356=
NR_051961.2:n.1152A=
NM_001267554.2:c.882A=	NP_001254483.1:p.Gly294=