Canonical Allele Identifier: CA1984668759

Gene: GAB2

Linked Data

• dbSNP Id: rs1258489378

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78380217_78380218insC , CM000673.2:g.78380217_78380218insC	GRCh38
NC_000011.9:g.78091263_78091264insC , CM000673.1:g.78091263_78091264insC	GRCh37
NC_000011.8:g.77768911_77768912insC	NCBI36
NG_016171.1:g.42605_42606insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.75+37428_75+37429insG MANE Select	ENSP00000354952.4:n.75+37428_75+37429insG
ENST00000361507.4:c.75+37428_75+37429insG	ENSP00000354952.4:n.75+37428_75+37429insG
ENST00000526030.1:n.177+37428_177+37429insG
ENST00000528886.5:c.-40+38019_-40+38020insG	ENSP00000433762.1:n.-40+38019_-40+38020insG
ENST00000530915.1:c.-127-16115_-127-16114insG	ENSP00000431868.1:n.-127-16115_-127-16114insG
ENST00000534823.1:n.126+37428_126+37429insG
NM_080491.2:c.75+37428_75+37429insG	NP_536739.1:n.75+37428_75+37429insG
XM_006718753.1:c.-127-16115_-127-16114insG	XP_006718816.1:n.-127-16115_-127-16114insG
XM_006718753.2:c.-127-16115_-127-16114insG	XP_006718816.1:n.-127-16115_-127-16114insG
NM_080491.3:c.75+37428_75+37429insG MANE Select	NP_536739.1:n.75+37428_75+37429insG