Canonical Allele Identifier: CA1984620979
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1866343781

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78281822_78281823del , CM000673.2:g.78281822_78281823del GRCh38
NC_000011.9:g.77992868_77992869del , CM000673.1:g.77992868_77992869del GRCh37
NC_000011.8:g.77670516_77670517del NCBI36
NG_016171.1:g.141002_141003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.76-920_76-919del MANE Select ENSP00000354952.4:n.76-920_76-919del
ENST00000340149.6:c.-39-920_-39-919del ENSP00000343959.2:n.-39-920_-39-919del
ENST00000361507.4:c.76-920_76-919del ENSP00000354952.4:n.76-920_76-919del
ENST00000526030.1:n.255-920_255-919del
ENST00000528886.5:c.-39-920_-39-919del ENSP00000433762.1:n.-39-920_-39-919del
ENST00000530915.1:c.-39-920_-39-919del ENSP00000431868.1:n.-39-920_-39-919del
ENST00000534823.1:n.127-920_127-919del
NM_012296.3:c.-39-920_-39-919del NP_036428.1:n.-39-920_-39-919del
NM_080491.2:c.76-920_76-919del NP_536739.1:n.76-920_76-919del
XM_006718753.1:c.-39-920_-39-919del XP_006718816.1:n.-39-920_-39-919del
XM_011545408.1:c.-341-920_-341-919del XP_011543710.1:n.-341-920_-341-919del
XM_006718753.2:c.-39-920_-39-919del XP_006718816.1:n.-39-920_-39-919del
XM_011545408.3:c.-341-920_-341-919del XP_011543710.1:n.-341-920_-341-919del
XM_024448782.1:c.22-920_22-919del XP_024304550.1:n.22-920_22-919del
NM_080491.3:c.76-920_76-919del MANE Select NP_536739.1:n.76-920_76-919del
NM_012296.4:c.-39-920_-39-919del NP_036428.1:n.-39-920_-39-919del