Canonical Allele Identifier: CA485423874

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772836G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118522G>A , CM000675.2:g.113118522G>A	GRCh38
NC_000013.10:g.113772836G>A , CM000675.1:g.113772836G>A	GRCh37
NC_000013.9:g.112820837G>A	NCBI36
NG_009258.1:g.724G>A , LRG_548:g.724G>A
NG_009262.1:g.17732G>A , LRG_554:g.17732G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.849G>A MANE Select	ENSP00000329546.4:p.Leu283=
ENST00000346342.7:c.849G>A	ENSP00000329546.3:p.Leu283=
ENST00000375581.3:c.915G>A	ENSP00000364731.3:p.Leu305=
ENST00000541084.5:c.663G>A	ENSP00000442051.2:p.Leu221=
NM_000131.4:c.915G>A , LRG_554t1:c.915G>A	NP_000122.1:p.Leu305=
NM_001267554.1:c.663G>A	NP_001254483.1:p.Leu221=
NM_019616.3:c.849G>A , LRG_554t2:c.849G>A	NP_062562.1:p.Leu283=
NR_051961.1:n.936G>A
XM_006719963.2:c.708G>A	XP_006720026.1:p.Leu236=
XM_011537474.1:c.957G>A	XP_011535776.1:p.Leu319=
XM_011537475.1:c.771G>A	XP_011535777.1:p.Leu257=
XM_011537476.1:c.609G>A	XP_011535778.1:p.Leu203=
XM_011537477.1:c.918G>A	XP_011535779.1:p.Leu306=
XM_006719963.3:c.753G>A	XP_006720026.2:p.Leu251=
XM_011537474.2:c.1002G>A	XP_011535776.2:p.Leu334=
XM_011537475.2:c.816G>A	XP_011535777.2:p.Leu272=
XM_011537476.2:c.609G>A	XP_011535778.1:p.Leu203=
NM_019616.4:c.849G>A MANE Select	NP_062562.1:p.Leu283=
NR_051961.2:n.933G>A
NM_001267554.2:c.663G>A	NP_001254483.1:p.Leu221=