Canonical Allele Identifier: CA1381558823
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87254352_87254357delinsACTTTT , CM000665.2:g.87254352_87254357delinsACTTTT GRCh38
NC_000003.11:g.87303502_87303507delinsACTTTT , CM000665.1:g.87303502_87303507delinsACTTTT GRCh37
NC_000003.10:g.87386192_87386197delinsACTTTT NCBI36
NG_007885.1:g.32090_32095delinsACTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263780.9:c.*530_*535delinsACTTTT MANE Select ENSP00000263780.4:n.*530_*535delinsACTTTT
ENST00000472024.3:c.*530_*535delinsACTTTT ENSP00000480032.2:n.*530_*535delinsACTTTT
ENST00000676705.1:c.*530_*535delinsACTTTT ENSP00000504098.1:n.*530_*535delinsACTTTT
ENST00000677929.1:n.4836_4841delinsACTTTT
ENST00000678859.1:n.4921_4926delinsACTTTT
ENST00000263780.8:c.*530_*535delinsACTTTT ENSP00000263780.4:n.*530_*535delinsACTTTT
ENST00000471660.5:c.*530_*535delinsACTTTT ENSP00000419998.1:n.*530_*535delinsACTTTT
NM_001244644.1:c.*530_*535delinsACTTTT NP_001231573.1:n.*530_*535delinsACTTTT
NM_014043.3:c.*530_*535delinsACTTTT NP_054762.2:n.*530_*535delinsACTTTT
XM_011533576.1:c.*530_*535delinsACTTTT XP_011531878.1:n.*530_*535delinsACTTTT
XM_011533576.2:c.*530_*535delinsACTTTT XP_011531878.1:n.*530_*535delinsACTTTT
NM_014043.4:c.*530_*535delinsACTTTT MANE Select NP_054762.2:n.*530_*535delinsACTTTT
NM_001244644.2:c.*530_*535delinsACTTTT NP_001231573.1:n.*530_*535delinsACTTTT