Canonical Allele Identifier: CA7059961

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113115708A>G , CM000675.2:g.113115708A>G	GRCh38
NC_000013.10:g.113770022A>G , CM000675.1:g.113770022A>G	GRCh37
NC_000013.9:g.112818023A>G	NCBI36
NG_009262.1:g.14918A>G , LRG_554:g.14918A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.413A>G MANE Select	NP_062562.1:p.Gln138Arg
ENST00000346342.8:c.413A>G MANE Select	ENSP00000329546.4:p.Gln138Arg
NM_000131.4:c.479A>G , LRG_554t1:c.479A>G	NP_000122.1:p.Gln160Arg
NM_001267554.1:c.227A>G	NP_001254483.1:p.Gln76Arg
NM_001267554.2:c.227A>G	NP_001254483.1:p.Gln76Arg
NM_019616.3:c.413A>G , LRG_554t2:c.413A>G	NP_062562.1:p.Gln138Arg
NR_051961.1:n.500A>G
NR_051961.2:n.497A>G
ENST00000346342.7:c.413A>G	ENSP00000329546.3:p.Gln138Arg
ENST00000375581.3:c.479A>G	ENSP00000364731.3:p.Gln160Arg
ENST00000444337.1:c.*221A>G	ENSP00000387669.1:n.*221A>G
ENST00000479674.1:n.698-1058A>G
ENST00000541084.5:c.227A>G	ENSP00000442051.2:p.Gln76Arg
XM_006719963.2:c.365-1058A>G	XP_006720026.1:n.365-1058A>G
XM_006719963.3:c.410-1058A>G	XP_006720026.2:n.410-1058A>G
XM_011537474.1:c.521A>G	XP_011535776.1:p.Gln174Arg
XM_011537474.2:c.566A>G	XP_011535776.2:p.Gln189Arg
XM_011537475.1:c.335A>G	XP_011535777.1:p.Gln112Arg
XM_011537475.2:c.380A>G	XP_011535777.2:p.Gln127Arg
XM_011537476.1:c.173A>G	XP_011535778.1:p.Gln58Arg
XM_011537476.2:c.173A>G	XP_011535778.1:p.Gln58Arg
XM_011537477.1:c.482A>G	XP_011535779.1:p.Gln161Arg