Canonical Allele Identifier: CA2623809720
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119132_113119133insC , CM000675.2:g.113119132_113119133insC GRCh38
NC_000013.10:g.113773446_113773447insC , CM000675.1:g.113773446_113773447insC GRCh37
NC_000013.9:g.112821447_112821448insC NCBI36
NG_009258.1:g.1334_1335insC , LRG_548:g.1334_1335insC
NG_009262.1:g.18342_18343insC , LRG_554:g.18342_18343insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*124_*125insC MANE Select ENSP00000329546.4:n.*124_*125insC
ENST00000346342.7:c.*124_*125insC ENSP00000329546.3:n.*124_*125insC
ENST00000375581.3:c.*124_*125insC ENSP00000364731.3:n.*124_*125insC
ENST00000541084.5:c.*124_*125insC ENSP00000442051.2:n.*124_*125insC
NM_000131.4:c.*124_*125insC , LRG_554t1:c.*124_*125insC NP_000122.1:n.*124_*125insC
NM_001267554.1:c.*124_*125insC NP_001254483.1:n.*124_*125insC
NM_019616.3:c.*124_*125insC , LRG_554t2:c.*124_*125insC NP_062562.1:n.*124_*125insC
NR_051961.1:n.1546_1547insC
XM_006719963.2:c.*124_*125insC XP_006720026.1:n.*124_*125insC
XM_011537474.1:c.*124_*125insC XP_011535776.1:n.*124_*125insC
XM_011537475.1:c.*124_*125insC XP_011535777.1:n.*124_*125insC
XM_011537476.1:c.*124_*125insC XP_011535778.1:n.*124_*125insC
XM_011537477.1:c.*124_*125insC XP_011535779.1:n.*124_*125insC
XM_006719963.3:c.*124_*125insC XP_006720026.2:n.*124_*125insC
XM_011537474.2:c.*124_*125insC XP_011535776.2:n.*124_*125insC
XM_011537475.2:c.*124_*125insC XP_011535777.2:n.*124_*125insC
XM_011537476.2:c.*124_*125insC XP_011535778.1:n.*124_*125insC
NM_019616.4:c.*124_*125insC MANE Select NP_062562.1:n.*124_*125insC
NR_051961.2:n.1543_1544insC
NM_001267554.2:c.*124_*125insC NP_001254483.1:n.*124_*125insC