Canonical Allele Identifier: CA485021185

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773118C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118804C>A , CM000675.2:g.113118804C>A	GRCh38
NC_000013.10:g.113773118C>A , CM000675.1:g.113773118C>A	GRCh37
NC_000013.9:g.112821119C>A	NCBI36
NG_009258.1:g.1006C>A , LRG_548:g.1006C>A
NG_009262.1:g.18014C>A , LRG_554:g.18014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1131C>A MANE Select	ENSP00000329546.4:p.Ser377=
ENST00000346342.7:c.1131C>A	ENSP00000329546.3:p.Ser377=
ENST00000375581.3:c.1197C>A	ENSP00000364731.3:p.Ser399=
ENST00000541084.5:c.945C>A	ENSP00000442051.2:p.Ser315=
NM_000131.4:c.1197C>A , LRG_554t1:c.1197C>A	NP_000122.1:p.Ser399=
NM_001267554.1:c.945C>A	NP_001254483.1:p.Ser315=
NM_019616.3:c.1131C>A , LRG_554t2:c.1131C>A	NP_062562.1:p.Ser377=
NR_051961.1:n.1218C>A
XM_006719963.2:c.990C>A	XP_006720026.1:p.Ser330=
XM_011537474.1:c.1239C>A	XP_011535776.1:p.Ser413=
XM_011537475.1:c.1053C>A	XP_011535777.1:p.Ser351=
XM_011537476.1:c.891C>A	XP_011535778.1:p.Ser297=
XM_011537477.1:c.1200C>A	XP_011535779.1:p.Ser400=
XM_006719963.3:c.1035C>A	XP_006720026.2:p.Ser345=
XM_011537474.2:c.1284C>A	XP_011535776.2:p.Ser428=
XM_011537475.2:c.1098C>A	XP_011535777.2:p.Ser366=
XM_011537476.2:c.891C>A	XP_011535778.1:p.Ser297=
NM_019616.4:c.1131C>A MANE Select	NP_062562.1:p.Ser377=
NR_051961.2:n.1215C>A
NM_001267554.2:c.945C>A	NP_001254483.1:p.Ser315=