Canonical Allele Identifier: CA485021741

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773307A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118993A>G , CM000675.2:g.113118993A>G	GRCh38
NC_000013.10:g.113773307A>G , CM000675.1:g.113773307A>G	GRCh37
NC_000013.9:g.112821308A>G	NCBI36
NG_009258.1:g.1195A>G , LRG_548:g.1195A>G
NG_009262.1:g.18203A>G , LRG_554:g.18203A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1320A>G MANE Select	ENSP00000329546.4:p.Arg440=
ENST00000346342.7:c.1320A>G	ENSP00000329546.3:p.Arg440=
ENST00000375581.3:c.1386A>G	ENSP00000364731.3:p.Arg462=
ENST00000541084.5:c.1134A>G	ENSP00000442051.2:p.Arg378=
NM_000131.4:c.1386A>G , LRG_554t1:c.1386A>G	NP_000122.1:p.Arg462=
NM_001267554.1:c.1134A>G	NP_001254483.1:p.Arg378=
NM_019616.3:c.1320A>G , LRG_554t2:c.1320A>G	NP_062562.1:p.Arg440=
NR_051961.1:n.1407A>G
XM_006719963.2:c.1179A>G	XP_006720026.1:p.Arg393=
XM_011537474.1:c.1428A>G	XP_011535776.1:p.Arg476=
XM_011537475.1:c.1242A>G	XP_011535777.1:p.Arg414=
XM_011537476.1:c.1080A>G	XP_011535778.1:p.Arg360=
XM_011537477.1:c.1389A>G	XP_011535779.1:p.Arg463=
XM_006719963.3:c.1224A>G	XP_006720026.2:p.Arg408=
XM_011537474.2:c.1473A>G	XP_011535776.2:p.Arg491=
XM_011537475.2:c.1287A>G	XP_011535777.2:p.Arg429=
XM_011537476.2:c.1080A>G	XP_011535778.1:p.Arg360=
NM_019616.4:c.1320A>G MANE Select	NP_062562.1:p.Arg440=
NR_051961.2:n.1404A>G
NM_001267554.2:c.1134A>G	NP_001254483.1:p.Arg378=