Canonical Allele Identifier: CA388786434

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773066A>G (hg19) ; chr13:g.113118752A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118752A>G , CM000675.2:g.113118752A>G	GRCh38
NC_000013.10:g.113773066A>G , CM000675.1:g.113773066A>G	GRCh37
NC_000013.9:g.112821067A>G	NCBI36
NG_009258.1:g.954A>G , LRG_548:g.954A>G
NG_009262.1:g.17962A>G , LRG_554:g.17962A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1079A>G MANE Select	ENSP00000329546.4:p.Asn360Ser
ENST00000346342.7:c.1079A>G	ENSP00000329546.3:p.Asn360Ser
ENST00000375581.3:c.1145A>G	ENSP00000364731.3:p.Asn382Ser
ENST00000541084.5:c.893A>G	ENSP00000442051.2:p.Asn298Ser
NM_000131.4:c.1145A>G , LRG_554t1:c.1145A>G	NP_000122.1:p.Asn382Ser
NM_001267554.1:c.893A>G	NP_001254483.1:p.Asn298Ser
NM_019616.3:c.1079A>G , LRG_554t2:c.1079A>G	NP_062562.1:p.Asn360Ser
NR_051961.1:n.1166A>G
XM_006719963.2:c.938A>G	XP_006720026.1:p.Asn313Ser
XM_011537474.1:c.1187A>G	XP_011535776.1:p.Asn396Ser
XM_011537475.1:c.1001A>G	XP_011535777.1:p.Asn334Ser
XM_011537476.1:c.839A>G	XP_011535778.1:p.Asn280Ser
XM_011537477.1:c.1148A>G	XP_011535779.1:p.Asn383Ser
XM_006719963.3:c.983A>G	XP_006720026.2:p.Asn328Ser
XM_011537474.2:c.1232A>G	XP_011535776.2:p.Asn411Ser
XM_011537475.2:c.1046A>G	XP_011535777.2:p.Asn349Ser
XM_011537476.2:c.839A>G	XP_011535778.1:p.Asn280Ser
NM_019616.4:c.1079A>G MANE Select	NP_062562.1:p.Asn360Ser
NR_051961.2:n.1163A>G
NM_001267554.2:c.893A>G	NP_001254483.1:p.Asn298Ser