Canonical Allele Identifier: CA918921344
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1565178931

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380086del , CM000673.2:g.78380086del GRCh38
NC_000011.9:g.78091132del , CM000673.1:g.78091132del GRCh37
NC_000011.8:g.77768780del NCBI36
NG_016171.1:g.42742del

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37565del MANE Select ENSP00000354952.4:n.75+37565del
ENST00000361507.4:c.75+37565del ENSP00000354952.4:n.75+37565del
ENST00000526030.1:n.177+37565del
ENST00000528886.5:c.-40+38156del ENSP00000433762.1:n.-40+38156del
ENST00000530915.1:c.-127-15978del ENSP00000431868.1:n.-127-15978del
ENST00000534823.1:n.126+37565del
NM_080491.2:c.75+37565del NP_536739.1:n.75+37565del
XM_006718753.1:c.-127-15978del XP_006718816.1:n.-127-15978del
XM_006718753.2:c.-127-15978del XP_006718816.1:n.-127-15978del
NM_080491.3:c.75+37565del MANE Select NP_536739.1:n.75+37565del