Canonical Allele Identifier: CA7059959

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113115698G>A , CM000675.2:g.113115698G>A	GRCh38
NC_000013.10:g.113770012G>A , CM000675.1:g.113770012G>A	GRCh37
NC_000013.9:g.112818013G>A	NCBI36
NG_009262.1:g.14908G>A , LRG_554:g.14908G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.403G>A MANE Select	NP_062562.1:p.Gly135Ser
ENST00000346342.8:c.403G>A MANE Select	ENSP00000329546.4:p.Gly135Ser
NM_000131.4:c.469G>A , LRG_554t1:c.469G>A	NP_000122.1:p.Gly157Ser
NM_001267554.1:c.217G>A	NP_001254483.1:p.Gly73Ser
NM_001267554.2:c.217G>A	NP_001254483.1:p.Gly73Ser
NM_019616.3:c.403G>A , LRG_554t2:c.403G>A	NP_062562.1:p.Gly135Ser
NR_051961.1:n.490G>A
NR_051961.2:n.487G>A
ENST00000346342.7:c.403G>A	ENSP00000329546.3:p.Gly135Ser
ENST00000375581.3:c.469G>A	ENSP00000364731.3:p.Gly157Ser
ENST00000444337.1:c.*211G>A	ENSP00000387669.1:n.*211G>A
ENST00000479674.1:n.698-1068G>A
ENST00000541084.5:c.217G>A	ENSP00000442051.2:p.Gly73Ser
XM_006719963.2:c.365-1068G>A	XP_006720026.1:n.365-1068G>A
XM_006719963.3:c.410-1068G>A	XP_006720026.2:n.410-1068G>A
XM_011537474.1:c.511G>A	XP_011535776.1:p.Gly171Ser
XM_011537474.2:c.556G>A	XP_011535776.2:p.Gly186Ser
XM_011537475.1:c.325G>A	XP_011535777.1:p.Gly109Ser
XM_011537475.2:c.370G>A	XP_011535777.2:p.Gly124Ser
XM_011537476.1:c.163G>A	XP_011535778.1:p.Gly55Ser
XM_011537476.2:c.163G>A	XP_011535778.1:p.Gly55Ser
XM_011537477.1:c.472G>A	XP_011535779.1:p.Gly158Ser