Canonical Allele Identifier: CA1381557929
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253279_87253281delinsTTA , CM000665.2:g.87253279_87253281delinsTTA GRCh38
NC_000003.11:g.87302429_87302431delinsTTA , CM000665.1:g.87302429_87302431delinsTTA GRCh37
NC_000003.10:g.87385119_87385121delinsTTA NCBI36
NG_007885.1:g.31017_31019delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263780.9:c.425-125_425-123delinsTTA MANE Select ENSP00000263780.4:n.425-125_425-123delinsTTA
ENST00000472024.3:c.473-125_473-123delinsTTA ENSP00000480032.2:n.473-125_473-123delinsTTA
ENST00000676705.1:c.473-125_473-123delinsTTA ENSP00000504098.1:n.473-125_473-123delinsTTA
ENST00000677929.1:n.3964_3966delinsTTA
ENST00000678859.1:n.4049_4051delinsTTA
ENST00000263780.8:c.425-125_425-123delinsTTA ENSP00000263780.4:n.425-125_425-123delinsTTA
ENST00000466696.1:n.231_233delinsTTA
ENST00000471660.5:c.302-125_302-123delinsTTA ENSP00000419998.1:n.302-125_302-123delinsTTA
ENST00000472024.2:c.473-125_473-123delinsTTA ENSP00000480032.1:n.473-125_473-123delinsTTA
ENST00000494980.5:c.335-125_335-123delinsTTA ENSP00000418920.1:n.335-125_335-123delinsTTA
NM_001244644.1:c.302-125_302-123delinsTTA NP_001231573.1:n.302-125_302-123delinsTTA
NM_014043.3:c.425-125_425-123delinsTTA NP_054762.2:n.425-125_425-123delinsTTA
XM_011533576.1:c.473-125_473-123delinsTTA XP_011531878.1:n.473-125_473-123delinsTTA
XM_011533576.2:c.473-125_473-123delinsTTA XP_011531878.1:n.473-125_473-123delinsTTA
NM_014043.4:c.425-125_425-123delinsTTA MANE Select NP_054762.2:n.425-125_425-123delinsTTA
NM_001244644.2:c.302-125_302-123delinsTTA NP_001231573.1:n.302-125_302-123delinsTTA