Canonical Allele Identifier: CA939853702
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1866342891

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78281781dup , CM000673.2:g.78281781dup GRCh38
NC_000011.9:g.77992827dup , CM000673.1:g.77992827dup GRCh37
NC_000011.8:g.77670475dup NCBI36
NG_016171.1:g.141042dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.76-880dup MANE Select ENSP00000354952.4:n.76-880dup
ENST00000340149.6:c.-39-880dup ENSP00000343959.2:n.-39-880dup
ENST00000361507.4:c.76-880dup ENSP00000354952.4:n.76-880dup
ENST00000526030.1:n.255-880dup
ENST00000528886.5:c.-39-880dup ENSP00000433762.1:n.-39-880dup
ENST00000530915.1:c.-39-880dup ENSP00000431868.1:n.-39-880dup
ENST00000534823.1:n.127-880dup
NM_012296.3:c.-39-880dup NP_036428.1:n.-39-880dup
NM_080491.2:c.76-880dup NP_536739.1:n.76-880dup
XM_006718753.1:c.-39-880dup XP_006718816.1:n.-39-880dup
XM_011545408.1:c.-341-880dup XP_011543710.1:n.-341-880dup
XM_006718753.2:c.-39-880dup XP_006718816.1:n.-39-880dup
XM_011545408.3:c.-341-880dup XP_011543710.1:n.-341-880dup
XM_024448782.1:c.22-880dup XP_024304550.1:n.22-880dup
NM_080491.3:c.76-880dup MANE Select NP_536739.1:n.76-880dup
NM_012296.4:c.-39-880dup NP_036428.1:n.-39-880dup