Canonical Allele Identifier: CA2523407359

Gene: GAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78342113_78342115dup , CM000673.2:g.78342113_78342115dup	GRCh38
NC_000011.9:g.78053159_78053161dup , CM000673.1:g.78053159_78053161dup	GRCh37
NC_000011.8:g.77730807_77730809dup	NCBI36
NG_016171.1:g.80708_80710dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000361507.5:c.76-61214_76-61212dup MANE Select	ENSP00000354952.4:n.76-61214_76-61212dup
ENST00000361507.4:c.76-61214_76-61212dup	ENSP00000354952.4:n.76-61214_76-61212dup
ENST00000526030.1:n.178-23896_178-23894dup
ENST00000528886.5:c.-39-61214_-39-61212dup	ENSP00000433762.1:n.-39-61214_-39-61212dup
ENST00000530915.1:c.-40+21901_-40+21903dup	ENSP00000431868.1:n.-40+21901_-40+21903dup
ENST00000534823.1:n.127-61214_127-61212dup
NM_080491.2:c.76-61214_76-61212dup	NP_536739.1:n.76-61214_76-61212dup
XM_006718753.1:c.-40+21901_-40+21903dup	XP_006718816.1:n.-40+21901_-40+21903dup
XM_006718753.2:c.-40+21901_-40+21903dup	XP_006718816.1:n.-40+21901_-40+21903dup
XM_024448782.1:c.21+12619_21+12621dup	XP_024304550.1:n.21+12619_21+12621dup
NM_080491.3:c.76-61214_76-61212dup MANE Select	NP_536739.1:n.76-61214_76-61212dup