Canonical Allele Identifier: CA2623810754
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119551_113119552insGATC , CM000675.2:g.113119551_113119552insGATC GRCh38
NC_000013.10:g.113773865_113773866insGATC , CM000675.1:g.113773865_113773866insGATC GRCh37
NC_000013.9:g.112821866_112821867insGATC NCBI36
NG_009258.1:g.1753_1754insGATC , LRG_548:g.1753_1754insGATC
NG_009262.1:g.18761_18762insGATC , LRG_554:g.18761_18762insGATC

Transcript Alleles

HGVS Amino-acid change
ENST00000346342.8:c.*543_*544insGATC MANE Select ENSP00000329546.4:n.*543_*544insGATC
ENST00000346342.7:c.*543_*544insGATC ENSP00000329546.3:n.*543_*544insGATC
ENST00000375581.3:c.*543_*544insGATC ENSP00000364731.3:n.*543_*544insGATC
ENST00000541084.5:c.*543_*544insGATC ENSP00000442051.2:n.*543_*544insGATC
NM_000131.4:c.*543_*544insGATC , LRG_554t1:c.*543_*544insGATC NP_000122.1:n.*543_*544insGATC
NM_001267554.1:c.*543_*544insGATC NP_001254483.1:n.*543_*544insGATC
NM_019616.3:c.*543_*544insGATC , LRG_554t2:c.*543_*544insGATC NP_062562.1:n.*543_*544insGATC
NR_051961.1:n.1965_1966insGATC
XM_006719963.2:c.*543_*544insGATC XP_006720026.1:n.*543_*544insGATC
XM_011537474.1:c.*543_*544insGATC XP_011535776.1:n.*543_*544insGATC
XM_011537475.1:c.*543_*544insGATC XP_011535777.1:n.*543_*544insGATC
XM_011537476.1:c.*543_*544insGATC XP_011535778.1:n.*543_*544insGATC
XM_011537477.1:c.*543_*544insGATC XP_011535779.1:n.*543_*544insGATC
XM_006719963.3:c.*543_*544insGATC XP_006720026.2:n.*543_*544insGATC
XM_011537474.2:c.*543_*544insGATC XP_011535776.2:n.*543_*544insGATC
XM_011537475.2:c.*543_*544insGATC XP_011535777.2:n.*543_*544insGATC
XM_011537476.2:c.*543_*544insGATC XP_011535778.1:n.*543_*544insGATC
NM_019616.4:c.*543_*544insGATC MANE Select NP_062562.1:n.*543_*544insGATC
NR_051961.2:n.1962_1963insGATC
NM_001267554.2:c.*543_*544insGATC NP_001254483.1:n.*543_*544insGATC