Canonical Allele Identifier: CA388786610

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773104G>A (hg19) ; chr13:g.113118790G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118790G>A , CM000675.2:g.113118790G>A	GRCh38
NC_000013.10:g.113773104G>A , CM000675.1:g.113773104G>A	GRCh37
NC_000013.9:g.112821105G>A	NCBI36
NG_009258.1:g.992G>A , LRG_548:g.992G>A
NG_009262.1:g.18000G>A , LRG_554:g.18000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1117G>A MANE Select	ENSP00000329546.4:p.Gly373Ser
ENST00000346342.7:c.1117G>A	ENSP00000329546.3:p.Gly373Ser
ENST00000375581.3:c.1183G>A	ENSP00000364731.3:p.Gly395Ser
ENST00000541084.5:c.931G>A	ENSP00000442051.2:p.Gly311Ser
NM_000131.4:c.1183G>A , LRG_554t1:c.1183G>A	NP_000122.1:p.Gly395Ser
NM_001267554.1:c.931G>A	NP_001254483.1:p.Gly311Ser
NM_019616.3:c.1117G>A , LRG_554t2:c.1117G>A	NP_062562.1:p.Gly373Ser
NR_051961.1:n.1204G>A
XM_006719963.2:c.976G>A	XP_006720026.1:p.Gly326Ser
XM_011537474.1:c.1225G>A	XP_011535776.1:p.Gly409Ser
XM_011537475.1:c.1039G>A	XP_011535777.1:p.Gly347Ser
XM_011537476.1:c.877G>A	XP_011535778.1:p.Gly293Ser
XM_011537477.1:c.1186G>A	XP_011535779.1:p.Gly396Ser
XM_006719963.3:c.1021G>A	XP_006720026.2:p.Gly341Ser
XM_011537474.2:c.1270G>A	XP_011535776.2:p.Gly424Ser
XM_011537475.2:c.1084G>A	XP_011535777.2:p.Gly362Ser
XM_011537476.2:c.877G>A	XP_011535778.1:p.Gly293Ser
NM_019616.4:c.1117G>A MANE Select	NP_062562.1:p.Gly373Ser
NR_051961.2:n.1201G>A
NM_001267554.2:c.931G>A	NP_001254483.1:p.Gly311Ser