Canonical Allele Identifier: CA388786720

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773126G>A (hg19) ; chr13:g.113118812G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118812G>A , CM000675.2:g.113118812G>A	GRCh38
NC_000013.10:g.113773126G>A , CM000675.1:g.113773126G>A	GRCh37
NC_000013.9:g.112821127G>A	NCBI36
NG_009258.1:g.1014G>A , LRG_548:g.1014G>A
NG_009262.1:g.18022G>A , LRG_554:g.18022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1139G>A MANE Select	ENSP00000329546.4:p.Gly380Glu
ENST00000346342.7:c.1139G>A	ENSP00000329546.3:p.Gly380Glu
ENST00000375581.3:c.1205G>A	ENSP00000364731.3:p.Gly402Glu
ENST00000541084.5:c.953G>A	ENSP00000442051.2:p.Gly318Glu
NM_000131.4:c.1205G>A , LRG_554t1:c.1205G>A	NP_000122.1:p.Gly402Glu
NM_001267554.1:c.953G>A	NP_001254483.1:p.Gly318Glu
NM_019616.3:c.1139G>A , LRG_554t2:c.1139G>A	NP_062562.1:p.Gly380Glu
NR_051961.1:n.1226G>A
XM_006719963.2:c.998G>A	XP_006720026.1:p.Gly333Glu
XM_011537474.1:c.1247G>A	XP_011535776.1:p.Gly416Glu
XM_011537475.1:c.1061G>A	XP_011535777.1:p.Gly354Glu
XM_011537476.1:c.899G>A	XP_011535778.1:p.Gly300Glu
XM_011537477.1:c.1208G>A	XP_011535779.1:p.Gly403Glu
XM_006719963.3:c.1043G>A	XP_006720026.2:p.Gly348Glu
XM_011537474.2:c.1292G>A	XP_011535776.2:p.Gly431Glu
XM_011537475.2:c.1106G>A	XP_011535777.2:p.Gly369Glu
XM_011537476.2:c.899G>A	XP_011535778.1:p.Gly300Glu
NM_019616.4:c.1139G>A MANE Select	NP_062562.1:p.Gly380Glu
NR_051961.2:n.1223G>A
NM_001267554.2:c.953G>A	NP_001254483.1:p.Gly318Glu