Canonical Allele Identifier: CA2666628933

Gene: CHMP2B

Linked Data

• gnomAD v4: 3-87254484-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87254486_87254487insGCA , CM000665.2:g.87254486_87254487insGCA	GRCh38
NC_000003.11:g.87303636_87303637insGCA , CM000665.1:g.87303636_87303637insGCA	GRCh37
NC_000003.10:g.87386326_87386327insGCA	NCBI36
NG_007885.1:g.32224_32225insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.*664_*665insGCA MANE Select	ENSP00000263780.4:n.*664_*665insGCA
ENST00000472024.3:c.*664_*665insGCA	ENSP00000480032.2:n.*664_*665insGCA
ENST00000676705.1:c.*664_*665insGCA	ENSP00000504098.1:n.*664_*665insGCA
ENST00000677929.1:n.4970_4971insGCA
ENST00000678859.1:n.5055_5056insGCA
ENST00000263780.8:c.*664_*665insGCA	ENSP00000263780.4:n.*664_*665insGCA
ENST00000471660.5:c.*664_*665insGCA	ENSP00000419998.1:n.*664_*665insGCA
NM_001244644.1:c.*664_*665insGCA	NP_001231573.1:n.*664_*665insGCA
NM_014043.3:c.*664_*665insGCA	NP_054762.2:n.*664_*665insGCA
XM_011533576.1:c.*664_*665insGCA	XP_011531878.1:n.*664_*665insGCA
XM_011533576.2:c.*664_*665insGCA	XP_011531878.1:n.*664_*665insGCA
NM_014043.4:c.*664_*665insGCA MANE Select	NP_054762.2:n.*664_*665insGCA
NM_001244644.2:c.*664_*665insGCA	NP_001231573.1:n.*664_*665insGCA