Canonical Allele Identifier: CA680553977

Gene: GAB2

Linked Data

• dbSNP Id: rs1265862983
• MyVariant Identifiers: chr11:g.78091141_78091142insAG (hg19) ; chr11:g.78380095_78380096insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78380100_78380101dup , CM000673.2:g.78380100_78380101dup	GRCh38
NC_000011.9:g.78091146_78091147dup , CM000673.1:g.78091146_78091147dup	GRCh37
NC_000011.8:g.77768794_77768795dup	NCBI36
NG_016171.1:g.42726_42727dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.75+37549_75+37550dup MANE Select	ENSP00000354952.4:n.75+37549_75+37550dup
ENST00000361507.4:c.75+37549_75+37550dup	ENSP00000354952.4:n.75+37549_75+37550dup
ENST00000526030.1:n.177+37549_177+37550dup
ENST00000528886.5:c.-40+38140_-40+38141dup	ENSP00000433762.1:n.-40+38140_-40+38141dup
ENST00000530915.1:c.-127-15994_-127-15993dup	ENSP00000431868.1:n.-127-15994_-127-15993dup
ENST00000534823.1:n.126+37549_126+37550dup
NM_080491.2:c.75+37549_75+37550dup	NP_536739.1:n.75+37549_75+37550dup
XM_006718753.1:c.-127-15994_-127-15993dup	XP_006718816.1:n.-127-15994_-127-15993dup
XM_006718753.2:c.-127-15994_-127-15993dup	XP_006718816.1:n.-127-15994_-127-15993dup
NM_080491.3:c.75+37549_75+37550dup MANE Select	NP_536739.1:n.75+37549_75+37550dup