Canonical Allele Identifier: CA7060163

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118517G>A , CM000675.2:g.113118517G>A	GRCh38
NC_000013.10:g.113772831G>A , CM000675.1:g.113772831G>A	GRCh37
NC_000013.9:g.112820832G>A	NCBI36
NG_009258.1:g.719G>A , LRG_548:g.719G>A
NG_009262.1:g.17727G>A , LRG_554:g.17727G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.844G>A MANE Select	NP_062562.1:p.Ala282Thr
ENST00000346342.8:c.844G>A MANE Select	ENSP00000329546.4:p.Ala282Thr
NM_000131.4:c.910G>A , LRG_554t1:c.910G>A	NP_000122.1:p.Ala304Thr
NM_001267554.1:c.658G>A	NP_001254483.1:p.Ala220Thr
NM_001267554.2:c.658G>A	NP_001254483.1:p.Ala220Thr
NM_019616.3:c.844G>A , LRG_554t2:c.844G>A	NP_062562.1:p.Ala282Thr
NR_051961.1:n.931G>A
NR_051961.2:n.928G>A
ENST00000346342.7:c.844G>A	ENSP00000329546.3:p.Ala282Thr
ENST00000375581.3:c.910G>A	ENSP00000364731.3:p.Ala304Thr
ENST00000541084.5:c.658G>A	ENSP00000442051.2:p.Ala220Thr
XM_006719963.2:c.703G>A	XP_006720026.1:p.Ala235Thr
XM_006719963.3:c.748G>A	XP_006720026.2:p.Ala250Thr
XM_011537474.1:c.952G>A	XP_011535776.1:p.Ala318Thr
XM_011537474.2:c.997G>A	XP_011535776.2:p.Ala333Thr
XM_011537475.1:c.766G>A	XP_011535777.1:p.Ala256Thr
XM_011537475.2:c.811G>A	XP_011535777.2:p.Ala271Thr
XM_011537476.1:c.604G>A	XP_011535778.1:p.Ala202Thr
XM_011537476.2:c.604G>A	XP_011535778.1:p.Ala202Thr
XM_011537477.1:c.913G>A	XP_011535779.1:p.Ala305Thr