Canonical Allele Identifier: CA388785827

Gene: F7

Linked Data

• gnomAD v4: 13-113118443-A-G
• MyVariant Identifiers: chr13:g.113772757A>G (hg19) ; chr13:g.113118443A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118443A>G , CM000675.2:g.113118443A>G	GRCh38
NC_000013.10:g.113772757A>G , CM000675.1:g.113772757A>G	GRCh37
NC_000013.9:g.112820758A>G	NCBI36
NG_009258.1:g.645A>G , LRG_548:g.645A>G
NG_009262.1:g.17653A>G , LRG_554:g.17653A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.770A>G MANE Select	ENSP00000329546.4:p.Asp257Gly
ENST00000346342.7:c.770A>G	ENSP00000329546.3:p.Asp257Gly
ENST00000375581.3:c.836A>G	ENSP00000364731.3:p.Asp279Gly
ENST00000541084.5:c.584A>G	ENSP00000442051.2:p.Asp195Gly
NM_000131.4:c.836A>G , LRG_554t1:c.836A>G	NP_000122.1:p.Asp279Gly
NM_001267554.1:c.584A>G	NP_001254483.1:p.Asp195Gly
NM_019616.3:c.770A>G , LRG_554t2:c.770A>G	NP_062562.1:p.Asp257Gly
NR_051961.1:n.857A>G
XM_006719963.2:c.629A>G	XP_006720026.1:p.Asp210Gly
XM_011537474.1:c.878A>G	XP_011535776.1:p.Asp293Gly
XM_011537475.1:c.692A>G	XP_011535777.1:p.Asp231Gly
XM_011537476.1:c.530A>G	XP_011535778.1:p.Asp177Gly
XM_011537477.1:c.839A>G	XP_011535779.1:p.Asp280Gly
XM_006719963.3:c.674A>G	XP_006720026.2:p.Asp225Gly
XM_011537474.2:c.923A>G	XP_011535776.2:p.Asp308Gly
XM_011537475.2:c.737A>G	XP_011535777.2:p.Asp246Gly
XM_011537476.2:c.530A>G	XP_011535778.1:p.Asp177Gly
NM_019616.4:c.770A>G MANE Select	NP_062562.1:p.Asp257Gly
NR_051961.2:n.854A>G
NM_001267554.2:c.584A>G	NP_001254483.1:p.Asp195Gly