Canonical Allele Identifier: CA388782491

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768260G>C (hg19) ; chr13:g.113113946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113946G>C , CM000675.2:g.113113946G>C	GRCh38
NC_000013.10:g.113768260G>C , CM000675.1:g.113768260G>C	GRCh37
NC_000013.9:g.112816261G>C	NCBI36
NG_009262.1:g.13156G>C , LRG_554:g.13156G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.350G>C MANE Select	ENSP00000329546.4:p.Arg117Pro
ENST00000346342.7:c.350G>C	ENSP00000329546.3:p.Arg117Pro
ENST00000375581.3:c.416G>C	ENSP00000364731.3:p.Arg139Pro
ENST00000444337.1:c.*158G>C	ENSP00000387669.1:n.*158G>C
ENST00000473085.1:n.297G>C
ENST00000479674.1:n.683G>C
ENST00000541084.5:c.164G>C	ENSP00000442051.2:p.Arg55Pro
NM_000131.4:c.416G>C , LRG_554t1:c.416G>C	NP_000122.1:p.Arg139Pro
NM_001267554.1:c.164G>C	NP_001254483.1:p.Arg55Pro
NM_019616.3:c.350G>C , LRG_554t2:c.350G>C	NP_062562.1:p.Arg117Pro
NR_051961.1:n.437G>C
XM_006719963.2:c.350G>C	XP_006720026.1:p.Arg117Pro
XM_011537474.1:c.350G>C	XP_011535776.1:p.Arg117Pro
XM_011537475.1:c.164G>C	XP_011535777.1:p.Arg55Pro
XM_011537477.1:c.311G>C	XP_011535779.1:p.Arg104Pro
XM_006719963.3:c.395G>C	XP_006720026.2:p.Arg132Pro
XM_011537474.2:c.395G>C	XP_011535776.2:p.Arg132Pro
XM_011537475.2:c.209G>C	XP_011535777.2:p.Arg70Pro
NM_019616.4:c.350G>C MANE Select	NP_062562.1:p.Arg117Pro
NR_051961.2:n.434G>C
NM_001267554.2:c.164G>C	NP_001254483.1:p.Arg55Pro