Canonical Allele Identifier: CA388785823

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772756G>A (hg19) ; chr13:g.113118442G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118442G>A , CM000675.2:g.113118442G>A	GRCh38
NC_000013.10:g.113772756G>A , CM000675.1:g.113772756G>A	GRCh37
NC_000013.9:g.112820757G>A	NCBI36
NG_009258.1:g.644G>A , LRG_548:g.644G>A
NG_009262.1:g.17652G>A , LRG_554:g.17652G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.769G>A MANE Select	ENSP00000329546.4:p.Asp257Asn
ENST00000346342.7:c.769G>A	ENSP00000329546.3:p.Asp257Asn
ENST00000375581.3:c.835G>A	ENSP00000364731.3:p.Asp279Asn
ENST00000541084.5:c.583G>A	ENSP00000442051.2:p.Asp195Asn
NM_000131.4:c.835G>A , LRG_554t1:c.835G>A	NP_000122.1:p.Asp279Asn
NM_001267554.1:c.583G>A	NP_001254483.1:p.Asp195Asn
NM_019616.3:c.769G>A , LRG_554t2:c.769G>A	NP_062562.1:p.Asp257Asn
NR_051961.1:n.856G>A
XM_006719963.2:c.628G>A	XP_006720026.1:p.Asp210Asn
XM_011537474.1:c.877G>A	XP_011535776.1:p.Asp293Asn
XM_011537475.1:c.691G>A	XP_011535777.1:p.Asp231Asn
XM_011537476.1:c.529G>A	XP_011535778.1:p.Asp177Asn
XM_011537477.1:c.838G>A	XP_011535779.1:p.Asp280Asn
XM_006719963.3:c.673G>A	XP_006720026.2:p.Asp225Asn
XM_011537474.2:c.922G>A	XP_011535776.2:p.Asp308Asn
XM_011537475.2:c.736G>A	XP_011535777.2:p.Asp246Asn
XM_011537476.2:c.529G>A	XP_011535778.1:p.Asp177Asn
NM_019616.4:c.769G>A MANE Select	NP_062562.1:p.Asp257Asn
NR_051961.2:n.853G>A
NM_001267554.2:c.583G>A	NP_001254483.1:p.Asp195Asn