Canonical Allele Identifier: CA485423845

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772788C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118474C>A , CM000675.2:g.113118474C>A	GRCh38
NC_000013.10:g.113772788C>A , CM000675.1:g.113772788C>A	GRCh37
NC_000013.9:g.112820789C>A	NCBI36
NG_009258.1:g.676C>A , LRG_548:g.676C>A
NG_009262.1:g.17684C>A , LRG_554:g.17684C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.801C>A MANE Select	ENSP00000329546.4:p.Ile267=
ENST00000346342.7:c.801C>A	ENSP00000329546.3:p.Ile267=
ENST00000375581.3:c.867C>A	ENSP00000364731.3:p.Ile289=
ENST00000541084.5:c.615C>A	ENSP00000442051.2:p.Ile205=
NM_000131.4:c.867C>A , LRG_554t1:c.867C>A	NP_000122.1:p.Ile289=
NM_001267554.1:c.615C>A	NP_001254483.1:p.Ile205=
NM_019616.3:c.801C>A , LRG_554t2:c.801C>A	NP_062562.1:p.Ile267=
NR_051961.1:n.888C>A
XM_006719963.2:c.660C>A	XP_006720026.1:p.Ile220=
XM_011537474.1:c.909C>A	XP_011535776.1:p.Ile303=
XM_011537475.1:c.723C>A	XP_011535777.1:p.Ile241=
XM_011537476.1:c.561C>A	XP_011535778.1:p.Ile187=
XM_011537477.1:c.870C>A	XP_011535779.1:p.Ile290=
XM_006719963.3:c.705C>A	XP_006720026.2:p.Ile235=
XM_011537474.2:c.954C>A	XP_011535776.2:p.Ile318=
XM_011537475.2:c.768C>A	XP_011535777.2:p.Ile256=
XM_011537476.2:c.561C>A	XP_011535778.1:p.Ile187=
NM_019616.4:c.801C>A MANE Select	NP_062562.1:p.Ile267=
NR_051961.2:n.885C>A
NM_001267554.2:c.615C>A	NP_001254483.1:p.Ile205=