Canonical Allele Identifier: CA485021686

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773298C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118984C>A , CM000675.2:g.113118984C>A	GRCh38
NC_000013.10:g.113773298C>A , CM000675.1:g.113773298C>A	GRCh37
NC_000013.9:g.112821299C>A	NCBI36
NG_009258.1:g.1186C>A , LRG_548:g.1186C>A
NG_009262.1:g.18194C>A , LRG_554:g.18194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1311C>A MANE Select	ENSP00000329546.4:p.Val437=
ENST00000346342.7:c.1311C>A	ENSP00000329546.3:p.Val437=
ENST00000375581.3:c.1377C>A	ENSP00000364731.3:p.Val459=
ENST00000541084.5:c.1125C>A	ENSP00000442051.2:p.Val375=
NM_000131.4:c.1377C>A , LRG_554t1:c.1377C>A	NP_000122.1:p.Val459=
NM_001267554.1:c.1125C>A	NP_001254483.1:p.Val375=
NM_019616.3:c.1311C>A , LRG_554t2:c.1311C>A	NP_062562.1:p.Val437=
NR_051961.1:n.1398C>A
XM_006719963.2:c.1170C>A	XP_006720026.1:p.Val390=
XM_011537474.1:c.1419C>A	XP_011535776.1:p.Val473=
XM_011537475.1:c.1233C>A	XP_011535777.1:p.Val411=
XM_011537476.1:c.1071C>A	XP_011535778.1:p.Val357=
XM_011537477.1:c.1380C>A	XP_011535779.1:p.Val460=
XM_006719963.3:c.1215C>A	XP_006720026.2:p.Val405=
XM_011537474.2:c.1464C>A	XP_011535776.2:p.Val488=
XM_011537475.2:c.1278C>A	XP_011535777.2:p.Val426=
XM_011537476.2:c.1071C>A	XP_011535778.1:p.Val357=
NM_019616.4:c.1311C>A MANE Select	NP_062562.1:p.Val437=
NR_051961.2:n.1395C>A
NM_001267554.2:c.1125C>A	NP_001254483.1:p.Val375=