Canonical Allele Identifier: CA388786011

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772852C>A (hg19) ; chr13:g.113118538C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118538C>A , CM000675.2:g.113118538C>A	GRCh38
NC_000013.10:g.113772852C>A , CM000675.1:g.113772852C>A	GRCh37
NC_000013.9:g.112820853C>A	NCBI36
NG_009258.1:g.740C>A , LRG_548:g.740C>A
NG_009262.1:g.17748C>A , LRG_554:g.17748C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.865C>A MANE Select	ENSP00000329546.4:p.Pro289Thr
ENST00000346342.7:c.865C>A	ENSP00000329546.3:p.Pro289Thr
ENST00000375581.3:c.931C>A	ENSP00000364731.3:p.Pro311Thr
ENST00000541084.5:c.679C>A	ENSP00000442051.2:p.Pro227Thr
NM_000131.4:c.931C>A , LRG_554t1:c.931C>A	NP_000122.1:p.Pro311Thr
NM_001267554.1:c.679C>A	NP_001254483.1:p.Pro227Thr
NM_019616.3:c.865C>A , LRG_554t2:c.865C>A	NP_062562.1:p.Pro289Thr
NR_051961.1:n.952C>A
XM_006719963.2:c.724C>A	XP_006720026.1:p.Pro242Thr
XM_011537474.1:c.973C>A	XP_011535776.1:p.Pro325Thr
XM_011537475.1:c.787C>A	XP_011535777.1:p.Pro263Thr
XM_011537476.1:c.625C>A	XP_011535778.1:p.Pro209Thr
XM_011537477.1:c.934C>A	XP_011535779.1:p.Pro312Thr
XM_006719963.3:c.769C>A	XP_006720026.2:p.Pro257Thr
XM_011537474.2:c.1018C>A	XP_011535776.2:p.Pro340Thr
XM_011537475.2:c.832C>A	XP_011535777.2:p.Pro278Thr
XM_011537476.2:c.625C>A	XP_011535778.1:p.Pro209Thr
NM_019616.4:c.865C>A MANE Select	NP_062562.1:p.Pro289Thr
NR_051961.2:n.949C>A
NM_001267554.2:c.679C>A	NP_001254483.1:p.Pro227Thr