Canonical Allele Identifier: CA388786433

Gene: F7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1079A>C MANE Select	ENSP00000329546.4:p.Asn360Thr
ENST00000346342.7:c.1079A>C	ENSP00000329546.3:p.Asn360Thr
ENST00000375581.3:c.1145A>C	ENSP00000364731.3:p.Asn382Thr
ENST00000541084.5:c.893A>C	ENSP00000442051.2:p.Asn298Thr
NM_000131.4:c.1145A>C , LRG_554t1:c.1145A>C	NP_000122.1:p.Asn382Thr
NM_001267554.1:c.893A>C	NP_001254483.1:p.Asn298Thr
NM_019616.3:c.1079A>C , LRG_554t2:c.1079A>C	NP_062562.1:p.Asn360Thr
NR_051961.1:n.1166A>C
XM_006719963.2:c.938A>C	XP_006720026.1:p.Asn313Thr
XM_011537474.1:c.1187A>C	XP_011535776.1:p.Asn396Thr
XM_011537475.1:c.1001A>C	XP_011535777.1:p.Asn334Thr
XM_011537476.1:c.839A>C	XP_011535778.1:p.Asn280Thr
XM_011537477.1:c.1148A>C	XP_011535779.1:p.Asn383Thr
XM_006719963.3:c.983A>C	XP_006720026.2:p.Asn328Thr
XM_011537474.2:c.1232A>C	XP_011535776.2:p.Asn411Thr
XM_011537475.2:c.1046A>C	XP_011535777.2:p.Asn349Thr
XM_011537476.2:c.839A>C	XP_011535778.1:p.Asn280Thr
NM_019616.4:c.1079A>C MANE Select	NP_062562.1:p.Asn360Thr
NR_051961.2:n.1163A>C
NM_001267554.2:c.893A>C	NP_001254483.1:p.Asn298Thr