Canonical Allele Identifier: CA485424000

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773013G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118699G>C , CM000675.2:g.113118699G>C	GRCh38
NC_000013.10:g.113773013G>C , CM000675.1:g.113773013G>C	GRCh37
NC_000013.9:g.112821014G>C	NCBI36
NG_009258.1:g.901G>C , LRG_548:g.901G>C
NG_009262.1:g.17909G>C , LRG_554:g.17909G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1026G>C MANE Select	ENSP00000329546.4:p.Arg342=
ENST00000346342.7:c.1026G>C	ENSP00000329546.3:p.Arg342=
ENST00000375581.3:c.1092G>C	ENSP00000364731.3:p.Arg364=
ENST00000541084.5:c.840G>C	ENSP00000442051.2:p.Arg280=
NM_000131.4:c.1092G>C , LRG_554t1:c.1092G>C	NP_000122.1:p.Arg364=
NM_001267554.1:c.840G>C	NP_001254483.1:p.Arg280=
NM_019616.3:c.1026G>C , LRG_554t2:c.1026G>C	NP_062562.1:p.Arg342=
NR_051961.1:n.1113G>C
XM_006719963.2:c.885G>C	XP_006720026.1:p.Arg295=
XM_011537474.1:c.1134G>C	XP_011535776.1:p.Arg378=
XM_011537475.1:c.948G>C	XP_011535777.1:p.Arg316=
XM_011537476.1:c.786G>C	XP_011535778.1:p.Arg262=
XM_011537477.1:c.1095G>C	XP_011535779.1:p.Arg365=
XM_006719963.3:c.930G>C	XP_006720026.2:p.Arg310=
XM_011537474.2:c.1179G>C	XP_011535776.2:p.Arg393=
XM_011537475.2:c.993G>C	XP_011535777.2:p.Arg331=
XM_011537476.2:c.786G>C	XP_011535778.1:p.Arg262=
NM_019616.4:c.1026G>C MANE Select	NP_062562.1:p.Arg342=
NR_051961.2:n.1110G>C
NM_001267554.2:c.840G>C	NP_001254483.1:p.Arg280=