Canonical Allele Identifier: CA918921346
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs11428219

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380226_78380227insTTTTTTTTTTTTTTTT , CM000673.2:g.78380226_78380227insTTTTTTTTTTTTTTTT GRCh38
NC_000011.9:g.78091272_78091273insTTTTTTTTTTTTTTTT , CM000673.1:g.78091272_78091273insTTTTTTTTTTTTTTTT GRCh37
NC_000011.8:g.77768920_77768921insTTTTTTTTTTTTTTTT NCBI36
NG_016171.1:g.42609_42610insAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37432_75+37433insAAAAAAAAAAAAAAAA MANE Select ENSP00000354952.4:n.75+37432_75+37433insAAAAAAAAAAAAAAAA
ENST00000361507.4:c.75+37432_75+37433insAAAAAAAAAAAAAAAA ENSP00000354952.4:n.75+37432_75+37433insAAAAAAAAAAAAAAAA
ENST00000526030.1:n.177+37432_177+37433insAAAAAAAAAAAAAAAA
ENST00000528886.5:c.-40+38023_-40+38024insAAAAAAAAAAAAAAAA ENSP00000433762.1:n.-40+38023_-40+38024insAAAAAAAAAAAAAAAA
ENST00000530915.1:c.-127-16111_-127-16110insAAAAAAAAAAAAAAAA ENSP00000431868.1:n.-127-16111_-127-16110insAAAAAAAAAAAAAAAA
ENST00000534823.1:n.126+37432_126+37433insAAAAAAAAAAAAAAAA
NM_080491.2:c.75+37432_75+37433insAAAAAAAAAAAAAAAA NP_536739.1:n.75+37432_75+37433insAAAAAAAAAAAAAAAA
XM_006718753.1:c.-127-16111_-127-16110insAAAAAAAAAAAAAAAA XP_006718816.1:n.-127-16111_-127-16110insAAAAAAAAAAAAAAAA
XM_006718753.2:c.-127-16111_-127-16110insAAAAAAAAAAAAAAAA XP_006718816.1:n.-127-16111_-127-16110insAAAAAAAAAAAAAAAA
NM_080491.3:c.75+37432_75+37433insAAAAAAAAAAAAAAAA MANE Select NP_536739.1:n.75+37432_75+37433insAAAAAAAAAAAAAAAA