Canonical Allele Identifier: CA2120141489
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118349C= , CM000675.2:g.113118349C= GRCh38
NC_000013.10:g.113772663C= , CM000675.1:g.113772663C= GRCh37
NC_000013.9:g.112820664C= NCBI36
NG_009258.1:g.551C= , LRG_548:g.551C=
NG_009262.1:g.17559C= , LRG_554:g.17559C=

Transcript Alleles

HGVS Amino-acid change
ENST00000346342.8:c.740-64C= MANE Select ENSP00000329546.4:n.740-64C=
ENST00000346342.7:c.740-64C= ENSP00000329546.3:n.740-64C=
ENST00000375581.3:c.806-64C= ENSP00000364731.3:n.806-64C=
ENST00000541084.5:c.554-64C= ENSP00000442051.2:n.554-64C=
NM_000131.4:c.806-64C= , LRG_554t1:c.806-64C= NP_000122.1:n.806-64C=
NM_001267554.1:c.554-64C= NP_001254483.1:n.554-64C=
NM_019616.3:c.740-64C= , LRG_554t2:c.740-64C= NP_062562.1:n.740-64C=
NR_051961.1:n.827-64C=
XM_006719963.2:c.599-64C= XP_006720026.1:n.599-64C=
XM_011537474.1:c.848-64C= XP_011535776.1:n.848-64C=
XM_011537475.1:c.662-64C= XP_011535777.1:n.662-64C=
XM_011537476.1:c.500-64C= XP_011535778.1:n.500-64C=
XM_011537477.1:c.809-64C= XP_011535779.1:n.809-64C=
XM_006719963.3:c.644-64C= XP_006720026.2:n.644-64C=
XM_011537474.2:c.893-64C= XP_011535776.2:n.893-64C=
XM_011537475.2:c.707-64C= XP_011535777.2:n.707-64C=
XM_011537476.2:c.500-64C= XP_011535778.1:n.500-64C=
NM_019616.4:c.740-64C= MANE Select NP_062562.1:n.740-64C=
NR_051961.2:n.824-64C=
NM_001267554.2:c.554-64C= NP_001254483.1:n.554-64C=