Canonical Allele Identifier: CA388782335
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113113910C>A , CM000675.2:g.113113910C>A GRCh38
NC_000013.10:g.113768224C>A , CM000675.1:g.113768224C>A GRCh37
NC_000013.9:g.112816225C>A NCBI36
NG_009262.1:g.13120C>A , LRG_554:g.13120C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.314C>A MANE Select ENSP00000329546.4:p.Ser105Tyr
ENST00000346342.7:c.314C>A ENSP00000329546.3:p.Ser105Tyr
ENST00000375581.3:c.380C>A ENSP00000364731.3:p.Ser127Tyr
ENST00000444337.1:c.*122C>A ENSP00000387669.1:n.*122C>A
ENST00000473085.1:n.261C>A
ENST00000479674.1:n.647C>A
ENST00000541084.5:c.128C>A ENSP00000442051.2:p.Ser43Tyr
NM_000131.4:c.380C>A , LRG_554t1:c.380C>A NP_000122.1:p.Ser127Tyr
NM_001267554.1:c.128C>A NP_001254483.1:p.Ser43Tyr
NM_019616.3:c.314C>A , LRG_554t2:c.314C>A NP_062562.1:p.Ser105Tyr
NR_051961.1:n.401C>A
XM_006719963.2:c.314C>A XP_006720026.1:p.Ser105Tyr
XM_011537474.1:c.314C>A XP_011535776.1:p.Ser105Tyr
XM_011537475.1:c.128C>A XP_011535777.1:p.Ser43Tyr
XM_011537477.1:c.275C>A XP_011535779.1:p.Ser92Tyr
XM_006719963.3:c.359C>A XP_006720026.2:p.Ser120Tyr
XM_011537474.2:c.359C>A XP_011535776.2:p.Ser120Tyr
XM_011537475.2:c.173C>A XP_011535777.2:p.Ser58Tyr
NM_019616.4:c.314C>A MANE Select NP_062562.1:p.Ser105Tyr
NR_051961.2:n.398C>A
NM_001267554.2:c.128C>A NP_001254483.1:p.Ser43Tyr