Canonical Allele Identifier: CA2120143932
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119488_113119490delinsCAG , CM000675.2:g.113119488_113119490delinsCAG GRCh38
NC_000013.10:g.113773802_113773804delinsCAG , CM000675.1:g.113773802_113773804delinsCAG GRCh37
NC_000013.9:g.112821803_112821805delinsCAG NCBI36
NG_009258.1:g.1690_1692delinsCAG , LRG_548:g.1690_1692delinsCAG
NG_009262.1:g.18698_18700delinsCAG , LRG_554:g.18698_18700delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*480_*482delinsCAG MANE Select ENSP00000329546.4:n.*480_*482delinsCAG
ENST00000346342.7:c.*480_*482delinsCAG ENSP00000329546.3:n.*480_*482delinsCAG
ENST00000375581.3:c.*480_*482delinsCAG ENSP00000364731.3:n.*480_*482delinsCAG
ENST00000541084.5:c.*480_*482delinsCAG ENSP00000442051.2:n.*480_*482delinsCAG
NM_000131.4:c.*480_*482delinsCAG , LRG_554t1:c.*480_*482delinsCAG NP_000122.1:n.*480_*482delinsCAG
NM_001267554.1:c.*480_*482delinsCAG NP_001254483.1:n.*480_*482delinsCAG
NM_019616.3:c.*480_*482delinsCAG , LRG_554t2:c.*480_*482delinsCAG NP_062562.1:n.*480_*482delinsCAG
NR_051961.1:n.1902_1904delinsCAG
XM_006719963.2:c.*480_*482delinsCAG XP_006720026.1:n.*480_*482delinsCAG
XM_011537474.1:c.*480_*482delinsCAG XP_011535776.1:n.*480_*482delinsCAG
XM_011537475.1:c.*480_*482delinsCAG XP_011535777.1:n.*480_*482delinsCAG
XM_011537476.1:c.*480_*482delinsCAG XP_011535778.1:n.*480_*482delinsCAG
XM_011537477.1:c.*480_*482delinsCAG XP_011535779.1:n.*480_*482delinsCAG
XM_006719963.3:c.*480_*482delinsCAG XP_006720026.2:n.*480_*482delinsCAG
XM_011537474.2:c.*480_*482delinsCAG XP_011535776.2:n.*480_*482delinsCAG
XM_011537475.2:c.*480_*482delinsCAG XP_011535777.2:n.*480_*482delinsCAG
XM_011537476.2:c.*480_*482delinsCAG XP_011535778.1:n.*480_*482delinsCAG
NM_019616.4:c.*480_*482delinsCAG MANE Select NP_062562.1:n.*480_*482delinsCAG
NR_051961.2:n.1899_1901delinsCAG
NM_001267554.2:c.*480_*482delinsCAG NP_001254483.1:n.*480_*482delinsCAG