Canonical Allele Identifier: CA2120135452
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113113800C= , CM000675.2:g.113113800C= GRCh38
NC_000013.10:g.113768114C= , CM000675.1:g.113768114C= GRCh37
NC_000013.9:g.112816115C= NCBI36
NG_009262.1:g.13010C= , LRG_554:g.13010C=

Transcript Alleles

HGVS Amino-acid change
ENST00000346342.8:c.250+24C= MANE Select ENSP00000329546.4:n.250+24C=
ENST00000346342.7:c.250+24C= ENSP00000329546.3:n.250+24C=
ENST00000375581.3:c.316+24C= ENSP00000364731.3:n.316+24C=
ENST00000444337.1:c.*12C= ENSP00000387669.1:n.*12C=
ENST00000473085.1:n.197+24C=
ENST00000479674.1:n.537C=
ENST00000541084.5:c.65-47C= ENSP00000442051.2:n.65-47C=
NM_000131.4:c.316+24C= , LRG_554t1:c.316+24C= NP_000122.1:n.316+24C=
NM_001267554.1:c.65-47C= NP_001254483.1:n.65-47C=
NM_019616.3:c.250+24C= , LRG_554t2:c.250+24C= NP_062562.1:n.250+24C=
NR_051961.1:n.291C=
XM_006719963.2:c.250+24C= XP_006720026.1:n.250+24C=
XM_011537474.1:c.250+24C= XP_011535776.1:n.250+24C=
XM_011537475.1:c.65-47C= XP_011535777.1:n.65-47C=
XM_011537477.1:c.212-47C= XP_011535779.1:n.212-47C=
XM_006719963.3:c.295+24C= XP_006720026.2:n.295+24C=
XM_011537474.2:c.295+24C= XP_011535776.2:n.295+24C=
XM_011537475.2:c.110-47C= XP_011535777.2:n.110-47C=
NM_019616.4:c.250+24C= MANE Select NP_062562.1:n.250+24C=
NR_051961.2:n.288C=
NM_001267554.2:c.65-47C= NP_001254483.1:n.65-47C=