Canonical Allele Identifier: CA388786718

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773125G>C (hg19) ; chr13:g.113118811G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118811G>C , CM000675.2:g.113118811G>C	GRCh38
NC_000013.10:g.113773125G>C , CM000675.1:g.113773125G>C	GRCh37
NC_000013.9:g.112821126G>C	NCBI36
NG_009258.1:g.1013G>C , LRG_548:g.1013G>C
NG_009262.1:g.18021G>C , LRG_554:g.18021G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1138G>C MANE Select	ENSP00000329546.4:p.Gly380Arg
ENST00000346342.7:c.1138G>C	ENSP00000329546.3:p.Gly380Arg
ENST00000375581.3:c.1204G>C	ENSP00000364731.3:p.Gly402Arg
ENST00000541084.5:c.952G>C	ENSP00000442051.2:p.Gly318Arg
NM_000131.4:c.1204G>C , LRG_554t1:c.1204G>C	NP_000122.1:p.Gly402Arg
NM_001267554.1:c.952G>C	NP_001254483.1:p.Gly318Arg
NM_019616.3:c.1138G>C , LRG_554t2:c.1138G>C	NP_062562.1:p.Gly380Arg
NR_051961.1:n.1225G>C
XM_006719963.2:c.997G>C	XP_006720026.1:p.Gly333Arg
XM_011537474.1:c.1246G>C	XP_011535776.1:p.Gly416Arg
XM_011537475.1:c.1060G>C	XP_011535777.1:p.Gly354Arg
XM_011537476.1:c.898G>C	XP_011535778.1:p.Gly300Arg
XM_011537477.1:c.1207G>C	XP_011535779.1:p.Gly403Arg
XM_006719963.3:c.1042G>C	XP_006720026.2:p.Gly348Arg
XM_011537474.2:c.1291G>C	XP_011535776.2:p.Gly431Arg
XM_011537475.2:c.1105G>C	XP_011535777.2:p.Gly369Arg
XM_011537476.2:c.898G>C	XP_011535778.1:p.Gly300Arg
NM_019616.4:c.1138G>C MANE Select	NP_062562.1:p.Gly380Arg
NR_051961.2:n.1222G>C
NM_001267554.2:c.952G>C	NP_001254483.1:p.Gly318Arg