Canonical Allele Identifier: CA388786218

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772955G>A (hg19) ; chr13:g.113118641G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118641G>A , CM000675.2:g.113118641G>A	GRCh38
NC_000013.10:g.113772955G>A , CM000675.1:g.113772955G>A	GRCh37
NC_000013.9:g.112820956G>A	NCBI36
NG_009258.1:g.843G>A , LRG_548:g.843G>A
NG_009262.1:g.17851G>A , LRG_554:g.17851G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.968G>A MANE Select	ENSP00000329546.4:p.Gly323Asp
ENST00000346342.7:c.968G>A	ENSP00000329546.3:p.Gly323Asp
ENST00000375581.3:c.1034G>A	ENSP00000364731.3:p.Gly345Asp
ENST00000541084.5:c.782G>A	ENSP00000442051.2:p.Gly261Asp
NM_000131.4:c.1034G>A , LRG_554t1:c.1034G>A	NP_000122.1:p.Gly345Asp
NM_001267554.1:c.782G>A	NP_001254483.1:p.Gly261Asp
NM_019616.3:c.968G>A , LRG_554t2:c.968G>A	NP_062562.1:p.Gly323Asp
NR_051961.1:n.1055G>A
XM_006719963.2:c.827G>A	XP_006720026.1:p.Gly276Asp
XM_011537474.1:c.1076G>A	XP_011535776.1:p.Gly359Asp
XM_011537475.1:c.890G>A	XP_011535777.1:p.Gly297Asp
XM_011537476.1:c.728G>A	XP_011535778.1:p.Gly243Asp
XM_011537477.1:c.1037G>A	XP_011535779.1:p.Gly346Asp
XM_006719963.3:c.872G>A	XP_006720026.2:p.Gly291Asp
XM_011537474.2:c.1121G>A	XP_011535776.2:p.Gly374Asp
XM_011537475.2:c.935G>A	XP_011535777.2:p.Gly312Asp
XM_011537476.2:c.728G>A	XP_011535778.1:p.Gly243Asp
NM_019616.4:c.968G>A MANE Select	NP_062562.1:p.Gly323Asp
NR_051961.2:n.1052G>A
NM_001267554.2:c.782G>A	NP_001254483.1:p.Gly261Asp