Canonical Allele Identifier: CA388786669

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773115C>G (hg19) ; chr13:g.113118801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118801C>G , CM000675.2:g.113118801C>G	GRCh38
NC_000013.10:g.113773115C>G , CM000675.1:g.113773115C>G	GRCh37
NC_000013.9:g.112821116C>G	NCBI36
NG_009258.1:g.1003C>G , LRG_548:g.1003C>G
NG_009262.1:g.18011C>G , LRG_554:g.18011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1128C>G MANE Select	ENSP00000329546.4:p.Asp376Glu
ENST00000346342.7:c.1128C>G	ENSP00000329546.3:p.Asp376Glu
ENST00000375581.3:c.1194C>G	ENSP00000364731.3:p.Asp398Glu
ENST00000541084.5:c.942C>G	ENSP00000442051.2:p.Asp314Glu
NM_000131.4:c.1194C>G , LRG_554t1:c.1194C>G	NP_000122.1:p.Asp398Glu
NM_001267554.1:c.942C>G	NP_001254483.1:p.Asp314Glu
NM_019616.3:c.1128C>G , LRG_554t2:c.1128C>G	NP_062562.1:p.Asp376Glu
NR_051961.1:n.1215C>G
XM_006719963.2:c.987C>G	XP_006720026.1:p.Asp329Glu
XM_011537474.1:c.1236C>G	XP_011535776.1:p.Asp412Glu
XM_011537475.1:c.1050C>G	XP_011535777.1:p.Asp350Glu
XM_011537476.1:c.888C>G	XP_011535778.1:p.Asp296Glu
XM_011537477.1:c.1197C>G	XP_011535779.1:p.Asp399Glu
XM_006719963.3:c.1032C>G	XP_006720026.2:p.Asp344Glu
XM_011537474.2:c.1281C>G	XP_011535776.2:p.Asp427Glu
XM_011537475.2:c.1095C>G	XP_011535777.2:p.Asp365Glu
XM_011537476.2:c.888C>G	XP_011535778.1:p.Asp296Glu
NM_019616.4:c.1128C>G MANE Select	NP_062562.1:p.Asp376Glu
NR_051961.2:n.1212C>G
NM_001267554.2:c.942C>G	NP_001254483.1:p.Asp314Glu