Canonical Allele Identifier: CA2120142264

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118651G= , CM000675.2:g.113118651G=	GRCh38
NC_000013.10:g.113772965G= , CM000675.1:g.113772965G=	GRCh37
NC_000013.9:g.112820966G=	NCBI36
NG_009258.1:g.853G= , LRG_548:g.853G=
NG_009262.1:g.17861G= , LRG_554:g.17861G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.978G= MANE Select	ENSP00000329546.4:p.Leu326=
ENST00000346342.7:c.978G=	ENSP00000329546.3:p.Leu326=
ENST00000375581.3:c.1044G=	ENSP00000364731.3:p.Leu348=
ENST00000541084.5:c.792G=	ENSP00000442051.2:p.Leu264=
NM_000131.4:c.1044G= , LRG_554t1:c.1044G=	NP_000122.1:p.Leu348=
NM_001267554.1:c.792G=	NP_001254483.1:p.Leu264=
NM_019616.3:c.978G= , LRG_554t2:c.978G=	NP_062562.1:p.Leu326=
NR_051961.1:n.1065G=
XM_006719963.2:c.837G=	XP_006720026.1:p.Leu279=
XM_011537474.1:c.1086G=	XP_011535776.1:p.Leu362=
XM_011537475.1:c.900G=	XP_011535777.1:p.Leu300=
XM_011537476.1:c.738G=	XP_011535778.1:p.Leu246=
XM_011537477.1:c.1047G=	XP_011535779.1:p.Leu349=
XM_006719963.3:c.882G=	XP_006720026.2:p.Leu294=
XM_011537474.2:c.1131G=	XP_011535776.2:p.Leu377=
XM_011537475.2:c.945G=	XP_011535777.2:p.Leu315=
XM_011537476.2:c.738G=	XP_011535778.1:p.Leu246=
NM_019616.4:c.978G= MANE Select	NP_062562.1:p.Leu326=
NR_051961.2:n.1062G=
NM_001267554.2:c.792G=	NP_001254483.1:p.Leu264=