Canonical Allele Identifier: CA2482717837

Gene: RAB29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774649_205774651delinsCAA , CM000663.2:g.205774649_205774651delinsCAA	GRCh38
NC_000001.10:g.205743777_205743779delinsCAA , CM000663.1:g.205743777_205743779delinsCAA	GRCh37
NC_000001.9:g.204010400_204010402delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.124+182_124+184delinsTTG MANE Select	ENSP00000356107.3:n.124+182_124+184delinsTTG
ENST00000235932.8:c.124+182_124+184delinsTTG	ENSP00000235932.4:n.124+182_124+184delinsTTG
ENST00000367139.7:c.124+182_124+184delinsTTG	ENSP00000356107.3:n.124+182_124+184delinsTTG
ENST00000414729.1:c.124+182_124+184delinsTTG	ENSP00000402910.1:n.124+182_124+184delinsTTG
ENST00000437324.6:c.-93+622_-93+624delinsTTG	ENSP00000416613.2:n.-93+622_-93+624delinsTTG
ENST00000446390.6:c.124+182_124+184delinsTTG	ENSP00000389899.2:n.124+182_124+184delinsTTG
ENST00000468887.1:n.168+622_168+624delinsTTG
ENST00000492534.1:n.319+182_319+184delinsTTG
ENST00000528078.1:c.124+182_124+184delinsTTG	ENSP00000431483.1:n.124+182_124+184delinsTTG
ENST00000533111.1:n.81+478_81+480delinsTTG
NM_001135662.1:c.124+182_124+184delinsTTG	NP_001129134.1:n.124+182_124+184delinsTTG
NM_001135663.1:c.124+182_124+184delinsTTG	NP_001129135.1:n.124+182_124+184delinsTTG
NM_001135664.1:c.-93+622_-93+624delinsTTG	NP_001129136.1:n.-93+622_-93+624delinsTTG
NM_003929.2:c.124+182_124+184delinsTTG	NP_003920.1:n.124+182_124+184delinsTTG
XM_005245569.1:c.124+182_124+184delinsTTG	XP_005245626.1:n.124+182_124+184delinsTTG
XM_005245570.1:c.124+182_124+184delinsTTG	XP_005245627.1:n.124+182_124+184delinsTTG
XM_005245571.1:c.124+182_124+184delinsTTG	XP_005245628.1:n.124+182_124+184delinsTTG
XM_006711605.2:c.-93+723_-93+725delinsTTG	XP_006711668.1:n.-93+723_-93+725delinsTTG
XM_006711606.1:c.-93+751_-93+753delinsTTG	XP_006711669.1:n.-93+751_-93+753delinsTTG
XM_006711605.3:c.-93+723_-93+725delinsTTG	XP_006711668.1:n.-93+723_-93+725delinsTTG
XM_006711606.3:c.-93+751_-93+753delinsTTG	XP_006711669.1:n.-93+751_-93+753delinsTTG
XM_017002748.1:c.124+182_124+184delinsTTG	XP_016858237.1:n.124+182_124+184delinsTTG
XM_017002749.1:c.124+182_124+184delinsTTG	XP_016858238.1:n.124+182_124+184delinsTTG
XM_017002750.1:c.124+182_124+184delinsTTG	XP_016858239.1:n.124+182_124+184delinsTTG
NM_003929.3:c.124+182_124+184delinsTTG MANE Select	NP_003920.1:n.124+182_124+184delinsTTG
NM_001135662.2:c.124+182_124+184delinsTTG	NP_001129134.1:n.124+182_124+184delinsTTG
NM_001135663.2:c.124+182_124+184delinsTTG	NP_001129135.1:n.124+182_124+184delinsTTG
NM_001135664.2:c.-93+622_-93+624delinsTTG	NP_001129136.1:n.-93+622_-93+624delinsTTG