Canonical Allele Identifier: CA2120142485

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118711G= , CM000675.2:g.113118711G=	GRCh38
NC_000013.10:g.113773025G= , CM000675.1:g.113773025G=	GRCh37
NC_000013.9:g.112821026G=	NCBI36
NG_009258.1:g.913G= , LRG_548:g.913G=
NG_009262.1:g.17921G= , LRG_554:g.17921G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1038G= MANE Select	ENSP00000329546.4:p.Gln346=
ENST00000346342.7:c.1038G=	ENSP00000329546.3:p.Gln346=
ENST00000375581.3:c.1104G=	ENSP00000364731.3:p.Gln368=
ENST00000541084.5:c.852G=	ENSP00000442051.2:p.Gln284=
NM_000131.4:c.1104G= , LRG_554t1:c.1104G=	NP_000122.1:p.Gln368=
NM_001267554.1:c.852G=	NP_001254483.1:p.Gln284=
NM_019616.3:c.1038G= , LRG_554t2:c.1038G=	NP_062562.1:p.Gln346=
NR_051961.1:n.1125G=
XM_006719963.2:c.897G=	XP_006720026.1:p.Gln299=
XM_011537474.1:c.1146G=	XP_011535776.1:p.Gln382=
XM_011537475.1:c.960G=	XP_011535777.1:p.Gln320=
XM_011537476.1:c.798G=	XP_011535778.1:p.Gln266=
XM_011537477.1:c.1107G=	XP_011535779.1:p.Gln369=
XM_006719963.3:c.942G=	XP_006720026.2:p.Gln314=
XM_011537474.2:c.1191G=	XP_011535776.2:p.Gln397=
XM_011537475.2:c.1005G=	XP_011535777.2:p.Gln335=
XM_011537476.2:c.798G=	XP_011535778.1:p.Gln266=
NM_019616.4:c.1038G= MANE Select	NP_062562.1:p.Gln346=
NR_051961.2:n.1122G=
NM_001267554.2:c.852G=	NP_001254483.1:p.Gln284=