Canonical Allele Identifier: CA388786766

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773135G>C (hg19) ; chr13:g.113118821G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118821G>C , CM000675.2:g.113118821G>C	GRCh38
NC_000013.10:g.113773135G>C , CM000675.1:g.113773135G>C	GRCh37
NC_000013.9:g.112821136G>C	NCBI36
NG_009258.1:g.1023G>C , LRG_548:g.1023G>C
NG_009262.1:g.18031G>C , LRG_554:g.18031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1148G>C MANE Select	ENSP00000329546.4:p.Gly383Ala
ENST00000346342.7:c.1148G>C	ENSP00000329546.3:p.Gly383Ala
ENST00000375581.3:c.1214G>C	ENSP00000364731.3:p.Gly405Ala
ENST00000541084.5:c.962G>C	ENSP00000442051.2:p.Gly321Ala
NM_000131.4:c.1214G>C , LRG_554t1:c.1214G>C	NP_000122.1:p.Gly405Ala
NM_001267554.1:c.962G>C	NP_001254483.1:p.Gly321Ala
NM_019616.3:c.1148G>C , LRG_554t2:c.1148G>C	NP_062562.1:p.Gly383Ala
NR_051961.1:n.1235G>C
XM_006719963.2:c.1007G>C	XP_006720026.1:p.Gly336Ala
XM_011537474.1:c.1256G>C	XP_011535776.1:p.Gly419Ala
XM_011537475.1:c.1070G>C	XP_011535777.1:p.Gly357Ala
XM_011537476.1:c.908G>C	XP_011535778.1:p.Gly303Ala
XM_011537477.1:c.1217G>C	XP_011535779.1:p.Gly406Ala
XM_006719963.3:c.1052G>C	XP_006720026.2:p.Gly351Ala
XM_011537474.2:c.1301G>C	XP_011535776.2:p.Gly434Ala
XM_011537475.2:c.1115G>C	XP_011535777.2:p.Gly372Ala
XM_011537476.2:c.908G>C	XP_011535778.1:p.Gly303Ala
NM_019616.4:c.1148G>C MANE Select	NP_062562.1:p.Gly383Ala
NR_051961.2:n.1232G>C
NM_001267554.2:c.962G>C	NP_001254483.1:p.Gly321Ala