Canonical Allele Identifier: CA2662732056
Gene: NBEAL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203016374_203016375insA , CM000664.2:g.203016374_203016375insA GRCh38
NC_000002.11:g.203881097_203881098insA , CM000664.1:g.203881097_203881098insA GRCh37
NC_000002.10:g.203589342_203589343insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000463830.2:n.334_335insA
ENST00000682077.1:n.336_337insA
ENST00000682333.1:n.334_335insA
ENST00000682787.1:c.-11_-10insA ENSP00000507858.1:n.-11_-10insA
ENST00000683091.1:c.-11_-10insA ENSP00000506951.1:n.-11_-10insA
ENST00000683927.1:n.323_324insA
ENST00000683969.1:c.-11_-10insA MANE Select ENSP00000508055.1:n.-11_-10insA
ENST00000449802.5:c.-11_-10insA ENSP00000399903.1:n.-11_-10insA
ENST00000460416.2:n.10_11insA
ENST00000478884.5:n.277_278insA
ENST00000492870.1:n.293_294insA
ENST00000497505.5:n.323_324insA
NM_001114132.1:c.-11_-10insA NP_001107604.1:n.-11_-10insA
XM_005246787.2:c.-11_-10insA XP_005246844.1:n.-11_-10insA
XM_006712698.2:c.-11_-10insA XP_006712761.1:n.-11_-10insA
XM_006712699.2:c.-11_-10insA XP_006712762.1:n.-11_-10insA
XM_006712700.2:c.-11_-10insA XP_006712763.1:n.-11_-10insA
XM_011511658.1:c.-11_-10insA XP_011509960.1:n.-11_-10insA
XM_011511659.1:c.-11_-10insA XP_011509961.1:n.-11_-10insA
XM_011511663.1:c.-11_-10insA XP_011509965.1:n.-11_-10insA
XM_011511664.1:c.-11_-10insA XP_011509966.1:n.-11_-10insA
XM_005246787.4:c.-11_-10insA XP_005246844.1:n.-11_-10insA
XM_006712698.4:c.-11_-10insA XP_006712761.1:n.-11_-10insA
XM_006712699.4:c.-11_-10insA XP_006712762.1:n.-11_-10insA
XM_011511658.3:c.-11_-10insA XP_011509960.1:n.-11_-10insA
XM_011511659.2:c.-11_-10insA XP_011509961.1:n.-11_-10insA
XM_011511663.3:c.-11_-10insA XP_011509965.1:n.-11_-10insA
NM_001114132.2:c.-11_-10insA NP_001107604.1:n.-11_-10insA
NM_001378026.1:c.-11_-10insA MANE Select NP_001364955.1:n.-11_-10insA