Canonical Allele Identifier: CA388785976

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772832C>G (hg19) ; chr13:g.113118518C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118518C>G , CM000675.2:g.113118518C>G	GRCh38
NC_000013.10:g.113772832C>G , CM000675.1:g.113772832C>G	GRCh37
NC_000013.9:g.112820833C>G	NCBI36
NG_009258.1:g.720C>G , LRG_548:g.720C>G
NG_009262.1:g.17728C>G , LRG_554:g.17728C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.845C>G MANE Select	ENSP00000329546.4:p.Ala282Gly
ENST00000346342.7:c.845C>G	ENSP00000329546.3:p.Ala282Gly
ENST00000375581.3:c.911C>G	ENSP00000364731.3:p.Ala304Gly
ENST00000541084.5:c.659C>G	ENSP00000442051.2:p.Ala220Gly
NM_000131.4:c.911C>G , LRG_554t1:c.911C>G	NP_000122.1:p.Ala304Gly
NM_001267554.1:c.659C>G	NP_001254483.1:p.Ala220Gly
NM_019616.3:c.845C>G , LRG_554t2:c.845C>G	NP_062562.1:p.Ala282Gly
NR_051961.1:n.932C>G
XM_006719963.2:c.704C>G	XP_006720026.1:p.Ala235Gly
XM_011537474.1:c.953C>G	XP_011535776.1:p.Ala318Gly
XM_011537475.1:c.767C>G	XP_011535777.1:p.Ala256Gly
XM_011537476.1:c.605C>G	XP_011535778.1:p.Ala202Gly
XM_011537477.1:c.914C>G	XP_011535779.1:p.Ala305Gly
XM_006719963.3:c.749C>G	XP_006720026.2:p.Ala250Gly
XM_011537474.2:c.998C>G	XP_011535776.2:p.Ala333Gly
XM_011537475.2:c.812C>G	XP_011535777.2:p.Ala271Gly
XM_011537476.2:c.605C>G	XP_011535778.1:p.Ala202Gly
NM_019616.4:c.845C>G MANE Select	NP_062562.1:p.Ala282Gly
NR_051961.2:n.929C>G
NM_001267554.2:c.659C>G	NP_001254483.1:p.Ala220Gly