Canonical Allele Identifier: CA1984668755
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380213_78380217delinsCTTTT , CM000673.2:g.78380213_78380217delinsCTTTT GRCh38
NC_000011.9:g.78091259_78091263delinsCTTTT , CM000673.1:g.78091259_78091263delinsCTTTT GRCh37
NC_000011.8:g.77768907_77768911delinsCTTTT NCBI36
NG_016171.1:g.42606_42610delinsAAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37429_75+37433delinsAAAAG MANE Select ENSP00000354952.4:n.75+37429_75+37433delinsAAAAG
ENST00000361507.4:c.75+37429_75+37433delinsAAAAG ENSP00000354952.4:n.75+37429_75+37433delinsAAAAG
ENST00000526030.1:n.177+37429_177+37433delinsAAAAG
ENST00000528886.5:c.-40+38020_-40+38024delinsAAAAG ENSP00000433762.1:n.-40+38020_-40+38024delinsAAAAG
ENST00000530915.1:c.-127-16114_-127-16110delinsAAAAG ENSP00000431868.1:n.-127-16114_-127-16110delinsAAAAG
ENST00000534823.1:n.126+37429_126+37433delinsAAAAG
NM_080491.2:c.75+37429_75+37433delinsAAAAG NP_536739.1:n.75+37429_75+37433delinsAAAAG
XM_006718753.1:c.-127-16114_-127-16110delinsAAAAG XP_006718816.1:n.-127-16114_-127-16110delinsAAAAG
XM_006718753.2:c.-127-16114_-127-16110delinsAAAAG XP_006718816.1:n.-127-16114_-127-16110delinsAAAAG
NM_080491.3:c.75+37429_75+37433delinsAAAAG MANE Select NP_536739.1:n.75+37429_75+37433delinsAAAAG