Canonical Allele Identifier: CA388787186

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773287C>G (hg19) ; chr13:g.113118973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118973C>G , CM000675.2:g.113118973C>G	GRCh38
NC_000013.10:g.113773287C>G , CM000675.1:g.113773287C>G	GRCh37
NC_000013.9:g.112821288C>G	NCBI36
NG_009258.1:g.1175C>G , LRG_548:g.1175C>G
NG_009262.1:g.18183C>G , LRG_554:g.18183C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1300C>G MANE Select	ENSP00000329546.4:p.Arg434Gly
ENST00000346342.7:c.1300C>G	ENSP00000329546.3:p.Arg434Gly
ENST00000375581.3:c.1366C>G	ENSP00000364731.3:p.Arg456Gly
ENST00000541084.5:c.1114C>G	ENSP00000442051.2:p.Arg372Gly
NM_000131.4:c.1366C>G , LRG_554t1:c.1366C>G	NP_000122.1:p.Arg456Gly
NM_001267554.1:c.1114C>G	NP_001254483.1:p.Arg372Gly
NM_019616.3:c.1300C>G , LRG_554t2:c.1300C>G	NP_062562.1:p.Arg434Gly
NR_051961.1:n.1387C>G
XM_006719963.2:c.1159C>G	XP_006720026.1:p.Arg387Gly
XM_011537474.1:c.1408C>G	XP_011535776.1:p.Arg470Gly
XM_011537475.1:c.1222C>G	XP_011535777.1:p.Arg408Gly
XM_011537476.1:c.1060C>G	XP_011535778.1:p.Arg354Gly
XM_011537477.1:c.1369C>G	XP_011535779.1:p.Arg457Gly
XM_006719963.3:c.1204C>G	XP_006720026.2:p.Arg402Gly
XM_011537474.2:c.1453C>G	XP_011535776.2:p.Arg485Gly
XM_011537475.2:c.1267C>G	XP_011535777.2:p.Arg423Gly
XM_011537476.2:c.1060C>G	XP_011535778.1:p.Arg354Gly
NM_019616.4:c.1300C>G MANE Select	NP_062562.1:p.Arg434Gly
NR_051961.2:n.1384C>G
NM_001267554.2:c.1114C>G	NP_001254483.1:p.Arg372Gly