Canonical Allele Identifier: CA1984621092

Gene: GAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78282076_78282079delinsTATG , CM000673.2:g.78282076_78282079delinsTATG	GRCh38
NC_000011.9:g.77993122_77993125delinsTATG , CM000673.1:g.77993122_77993125delinsTATG	GRCh37
NC_000011.8:g.77670770_77670773delinsTATG	NCBI36
NG_016171.1:g.140744_140747delinsCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.76-1178_76-1175delinsCATA MANE Select	ENSP00000354952.4:n.76-1178_76-1175delinsCATA
ENST00000340149.6:c.-39-1178_-39-1175delinsCATA	ENSP00000343959.2:n.-39-1178_-39-1175delinsCATA
ENST00000361507.4:c.76-1178_76-1175delinsCATA	ENSP00000354952.4:n.76-1178_76-1175delinsCATA
ENST00000526030.1:n.255-1178_255-1175delinsCATA
ENST00000528886.5:c.-39-1178_-39-1175delinsCATA	ENSP00000433762.1:n.-39-1178_-39-1175delinsCATA
ENST00000530915.1:c.-39-1178_-39-1175delinsCATA	ENSP00000431868.1:n.-39-1178_-39-1175delinsCATA
ENST00000534823.1:n.127-1178_127-1175delinsCATA
NM_012296.3:c.-39-1178_-39-1175delinsCATA	NP_036428.1:n.-39-1178_-39-1175delinsCATA
NM_080491.2:c.76-1178_76-1175delinsCATA	NP_536739.1:n.76-1178_76-1175delinsCATA
XM_006718753.1:c.-39-1178_-39-1175delinsCATA	XP_006718816.1:n.-39-1178_-39-1175delinsCATA
XM_011545408.1:c.-341-1178_-341-1175delinsCATA	XP_011543710.1:n.-341-1178_-341-1175delinsCATA
XM_006718753.2:c.-39-1178_-39-1175delinsCATA	XP_006718816.1:n.-39-1178_-39-1175delinsCATA
XM_011545408.3:c.-341-1178_-341-1175delinsCATA	XP_011543710.1:n.-341-1178_-341-1175delinsCATA
XM_024448782.1:c.22-1178_22-1175delinsCATA	XP_024304550.1:n.22-1178_22-1175delinsCATA
NM_080491.3:c.76-1178_76-1175delinsCATA MANE Select	NP_536739.1:n.76-1178_76-1175delinsCATA
NM_012296.4:c.-39-1178_-39-1175delinsCATA	NP_036428.1:n.-39-1178_-39-1175delinsCATA