Canonical Allele Identifier: CA1984646500

Gene: GAB2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78334025G>T , CM000673.2:g.78334025G>T	GRCh38
NC_000011.9:g.78045071G>T , CM000673.1:g.78045071G>T	GRCh37
NC_000011.8:g.77722719G>T	NCBI36
NG_016171.1:g.88798C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.76-53124C>A MANE Select	ENSP00000354952.4:n.76-53124C>A
ENST00000340149.6:c.-40+7735C>A	ENSP00000343959.2:n.-40+7735C>A
ENST00000361507.4:c.76-53124C>A	ENSP00000354952.4:n.76-53124C>A
ENST00000526030.1:n.178-15806C>A
ENST00000528886.5:c.-39-53124C>A	ENSP00000433762.1:n.-39-53124C>A
ENST00000530915.1:c.-40+29991C>A	ENSP00000431868.1:n.-40+29991C>A
ENST00000534823.1:n.127-53124C>A
NM_012296.3:c.-40+7735C>A	NP_036428.1:n.-40+7735C>A
NM_080491.2:c.76-53124C>A	NP_536739.1:n.76-53124C>A
XM_006718753.1:c.-40+29991C>A	XP_006718816.1:n.-40+29991C>A
XM_006718753.2:c.-40+29991C>A	XP_006718816.1:n.-40+29991C>A
XM_024448782.1:c.21+20709C>A	XP_024304550.1:n.21+20709C>A
NM_080491.3:c.76-53124C>A MANE Select	NP_536739.1:n.76-53124C>A
NM_012296.4:c.-40+7735C>A	NP_036428.1:n.-40+7735C>A