Canonical Allele Identifier: CA7060140

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118454C>T , CM000675.2:g.113118454C>T	GRCh38
NC_000013.10:g.113772768C>T , CM000675.1:g.113772768C>T	GRCh37
NC_000013.9:g.112820769C>T	NCBI36
NG_009258.1:g.656C>T , LRG_548:g.656C>T
NG_009262.1:g.17664C>T , LRG_554:g.17664C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.781C>T MANE Select	NP_062562.1:p.Arg261Trp
ENST00000346342.8:c.781C>T MANE Select	ENSP00000329546.4:p.Arg261Trp
NM_000131.4:c.847C>T , LRG_554t1:c.847C>T	NP_000122.1:p.Arg283Trp
NM_001267554.1:c.595C>T	NP_001254483.1:p.Arg199Trp
NM_001267554.2:c.595C>T	NP_001254483.1:p.Arg199Trp
NM_019616.3:c.781C>T , LRG_554t2:c.781C>T	NP_062562.1:p.Arg261Trp
NR_051961.1:n.868C>T
NR_051961.2:n.865C>T
ENST00000346342.7:c.781C>T	ENSP00000329546.3:p.Arg261Trp
ENST00000375581.3:c.847C>T	ENSP00000364731.3:p.Arg283Trp
ENST00000541084.5:c.595C>T	ENSP00000442051.2:p.Arg199Trp
XM_006719963.2:c.640C>T	XP_006720026.1:p.Arg214Trp
XM_006719963.3:c.685C>T	XP_006720026.2:p.Arg229Trp
XM_011537474.1:c.889C>T	XP_011535776.1:p.Arg297Trp
XM_011537474.2:c.934C>T	XP_011535776.2:p.Arg312Trp
XM_011537475.1:c.703C>T	XP_011535777.1:p.Arg235Trp
XM_011537475.2:c.748C>T	XP_011535777.2:p.Arg250Trp
XM_011537476.1:c.541C>T	XP_011535778.1:p.Arg181Trp
XM_011537476.2:c.541C>T	XP_011535778.1:p.Arg181Trp
XM_011537477.1:c.850C>T	XP_011535779.1:p.Arg284Trp