Canonical Allele Identifier: CA388786220

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772957C>G (hg19) ; chr13:g.113118643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118643C>G , CM000675.2:g.113118643C>G	GRCh38
NC_000013.10:g.113772957C>G , CM000675.1:g.113772957C>G	GRCh37
NC_000013.9:g.112820958C>G	NCBI36
NG_009258.1:g.845C>G , LRG_548:g.845C>G
NG_009262.1:g.17853C>G , LRG_554:g.17853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.970C>G MANE Select	ENSP00000329546.4:p.Gln324Glu
ENST00000346342.7:c.970C>G	ENSP00000329546.3:p.Gln324Glu
ENST00000375581.3:c.1036C>G	ENSP00000364731.3:p.Gln346Glu
ENST00000541084.5:c.784C>G	ENSP00000442051.2:p.Gln262Glu
NM_000131.4:c.1036C>G , LRG_554t1:c.1036C>G	NP_000122.1:p.Gln346Glu
NM_001267554.1:c.784C>G	NP_001254483.1:p.Gln262Glu
NM_019616.3:c.970C>G , LRG_554t2:c.970C>G	NP_062562.1:p.Gln324Glu
NR_051961.1:n.1057C>G
XM_006719963.2:c.829C>G	XP_006720026.1:p.Gln277Glu
XM_011537474.1:c.1078C>G	XP_011535776.1:p.Gln360Glu
XM_011537475.1:c.892C>G	XP_011535777.1:p.Gln298Glu
XM_011537476.1:c.730C>G	XP_011535778.1:p.Gln244Glu
XM_011537477.1:c.1039C>G	XP_011535779.1:p.Gln347Glu
XM_006719963.3:c.874C>G	XP_006720026.2:p.Gln292Glu
XM_011537474.2:c.1123C>G	XP_011535776.2:p.Gln375Glu
XM_011537475.2:c.937C>G	XP_011535777.2:p.Gln313Glu
XM_011537476.2:c.730C>G	XP_011535778.1:p.Gln244Glu
NM_019616.4:c.970C>G MANE Select	NP_062562.1:p.Gln324Glu
NR_051961.2:n.1054C>G
NM_001267554.2:c.784C>G	NP_001254483.1:p.Gln262Glu