Canonical Allele Identifier: CA485021191

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773127G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118813G>C , CM000675.2:g.113118813G>C	GRCh38
NC_000013.10:g.113773127G>C , CM000675.1:g.113773127G>C	GRCh37
NC_000013.9:g.112821128G>C	NCBI36
NG_009258.1:g.1015G>C , LRG_548:g.1015G>C
NG_009262.1:g.18023G>C , LRG_554:g.18023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1140G>C MANE Select	ENSP00000329546.4:p.Gly380=
ENST00000346342.7:c.1140G>C	ENSP00000329546.3:p.Gly380=
ENST00000375581.3:c.1206G>C	ENSP00000364731.3:p.Gly402=
ENST00000541084.5:c.954G>C	ENSP00000442051.2:p.Gly318=
NM_000131.4:c.1206G>C , LRG_554t1:c.1206G>C	NP_000122.1:p.Gly402=
NM_001267554.1:c.954G>C	NP_001254483.1:p.Gly318=
NM_019616.3:c.1140G>C , LRG_554t2:c.1140G>C	NP_062562.1:p.Gly380=
NR_051961.1:n.1227G>C
XM_006719963.2:c.999G>C	XP_006720026.1:p.Gly333=
XM_011537474.1:c.1248G>C	XP_011535776.1:p.Gly416=
XM_011537475.1:c.1062G>C	XP_011535777.1:p.Gly354=
XM_011537476.1:c.900G>C	XP_011535778.1:p.Gly300=
XM_011537477.1:c.1209G>C	XP_011535779.1:p.Gly403=
XM_006719963.3:c.1044G>C	XP_006720026.2:p.Gly348=
XM_011537474.2:c.1293G>C	XP_011535776.2:p.Gly431=
XM_011537475.2:c.1107G>C	XP_011535777.2:p.Gly369=
XM_011537476.2:c.900G>C	XP_011535778.1:p.Gly300=
NM_019616.4:c.1140G>C MANE Select	NP_062562.1:p.Gly380=
NR_051961.2:n.1224G>C
NM_001267554.2:c.954G>C	NP_001254483.1:p.Gly318=