Canonical Allele Identifier: CA388785931

Gene: F7

Linked Data

• gnomAD v4: 13-113118497-G-A
• MyVariant Identifiers: chr13:g.113772811G>A (hg19) ; chr13:g.113118497G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118497G>A , CM000675.2:g.113118497G>A	GRCh38
NC_000013.10:g.113772811G>A , CM000675.1:g.113772811G>A	GRCh37
NC_000013.9:g.112820812G>A	NCBI36
NG_009258.1:g.699G>A , LRG_548:g.699G>A
NG_009262.1:g.17707G>A , LRG_554:g.17707G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.824G>A MANE Select	ENSP00000329546.4:p.Gly275Asp
ENST00000346342.7:c.824G>A	ENSP00000329546.3:p.Gly275Asp
ENST00000375581.3:c.890G>A	ENSP00000364731.3:p.Gly297Asp
ENST00000541084.5:c.638G>A	ENSP00000442051.2:p.Gly213Asp
NM_000131.4:c.890G>A , LRG_554t1:c.890G>A	NP_000122.1:p.Gly297Asp
NM_001267554.1:c.638G>A	NP_001254483.1:p.Gly213Asp
NM_019616.3:c.824G>A , LRG_554t2:c.824G>A	NP_062562.1:p.Gly275Asp
NR_051961.1:n.911G>A
XM_006719963.2:c.683G>A	XP_006720026.1:p.Gly228Asp
XM_011537474.1:c.932G>A	XP_011535776.1:p.Gly311Asp
XM_011537475.1:c.746G>A	XP_011535777.1:p.Gly249Asp
XM_011537476.1:c.584G>A	XP_011535778.1:p.Gly195Asp
XM_011537477.1:c.893G>A	XP_011535779.1:p.Gly298Asp
XM_006719963.3:c.728G>A	XP_006720026.2:p.Gly243Asp
XM_011537474.2:c.977G>A	XP_011535776.2:p.Gly326Asp
XM_011537475.2:c.791G>A	XP_011535777.2:p.Gly264Asp
XM_011537476.2:c.584G>A	XP_011535778.1:p.Gly195Asp
NM_019616.4:c.824G>A MANE Select	NP_062562.1:p.Gly275Asp
NR_051961.2:n.908G>A
NM_001267554.2:c.638G>A	NP_001254483.1:p.Gly213Asp