Canonical Allele Identifier: CA388782480

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768257G>T (hg19) ; chr13:g.113113943G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113943G>T , CM000675.2:g.113113943G>T	GRCh38
NC_000013.10:g.113768257G>T , CM000675.1:g.113768257G>T	GRCh37
NC_000013.9:g.112816258G>T	NCBI36
NG_009262.1:g.13153G>T , LRG_554:g.13153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.347G>T MANE Select	ENSP00000329546.4:p.Gly116Val
ENST00000346342.7:c.347G>T	ENSP00000329546.3:p.Gly116Val
ENST00000375581.3:c.413G>T	ENSP00000364731.3:p.Gly138Val
ENST00000444337.1:c.*155G>T	ENSP00000387669.1:n.*155G>T
ENST00000473085.1:n.294G>T
ENST00000479674.1:n.680G>T
ENST00000541084.5:c.161G>T	ENSP00000442051.2:p.Gly54Val
NM_000131.4:c.413G>T , LRG_554t1:c.413G>T	NP_000122.1:p.Gly138Val
NM_001267554.1:c.161G>T	NP_001254483.1:p.Gly54Val
NM_019616.3:c.347G>T , LRG_554t2:c.347G>T	NP_062562.1:p.Gly116Val
NR_051961.1:n.434G>T
XM_006719963.2:c.347G>T	XP_006720026.1:p.Gly116Val
XM_011537474.1:c.347G>T	XP_011535776.1:p.Gly116Val
XM_011537475.1:c.161G>T	XP_011535777.1:p.Gly54Val
XM_011537477.1:c.308G>T	XP_011535779.1:p.Gly103Val
XM_006719963.3:c.392G>T	XP_006720026.2:p.Gly131Val
XM_011537474.2:c.392G>T	XP_011535776.2:p.Gly131Val
XM_011537475.2:c.206G>T	XP_011535777.2:p.Gly69Val
NM_019616.4:c.347G>T MANE Select	NP_062562.1:p.Gly116Val
NR_051961.2:n.431G>T
NM_001267554.2:c.161G>T	NP_001254483.1:p.Gly54Val