Canonical Allele Identifier: CA2178720767

Gene: RAB27A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55223870_55223878delinsTCTCCACAA , CM000677.2:g.55223870_55223878delinsTCTCCACAA	GRCh38
NC_000015.9:g.55516068_55516076delinsTCTCCACAA , CM000677.1:g.55516068_55516076delinsTCTCCACAA	GRCh37
NC_000015.8:g.53303360_53303368delinsTCTCCACAA	NCBI36
NG_009103.1:g.70926_70934delinsTTGTGGAGA , LRG_96:g.70926_70934delinsTTGTGGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697641.1:n.2503+11_2503+19delinsTTGTGGAGA
ENST00000697642.1:c.467+11_467+19delinsTTGTGGAGA	ENSP00000513368.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000697643.1:c.467+11_467+19delinsTTGTGGAGA	ENSP00000513369.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000697644.1:n.2635+11_2635+19delinsTTGTGGAGA
ENST00000336787.6:c.467+11_467+19delinsTTGTGGAGA MANE Select	ENSP00000337761.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000336787.5:c.467+11_467+19delinsTTGTGGAGA	ENSP00000337761.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000396307.6:c.467+11_467+19delinsTTGTGGAGA	ENSP00000379601.2:n.467+11_467+19delinsTTGTGGAGA
ENST00000564609.5:c.467+11_467+19delinsTTGTGGAGA	ENSP00000455012.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000566877.5:c.467+11_467+19delinsTTGTGGAGA	ENSP00000454695.1:n.467+11_467+19delinsTTGTGGAGA
ENST00000569493.5:c.467+11_467+19delinsTTGTGGAGA	ENSP00000456059.1:n.467+11_467+19delinsTTGTGGAGA
NM_004580.4:c.467+11_467+19delinsTTGTGGAGA	NP_004571.2:n.467+11_467+19delinsTTGTGGAGA
NM_183234.2:c.467+11_467+19delinsTTGTGGAGA	NP_899057.1:n.467+11_467+19delinsTTGTGGAGA
NM_183235.2:c.467+11_467+19delinsTTGTGGAGA	NP_899058.1:n.467+11_467+19delinsTTGTGGAGA
NM_183236.2:c.467+11_467+19delinsTTGTGGAGA	NP_899059.1:n.467+11_467+19delinsTTGTGGAGA
XM_005254576.3:c.467+11_467+19delinsTTGTGGAGA	XP_005254633.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521852.1:c.467+11_467+19delinsTTGTGGAGA	XP_011520154.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521853.1:c.467+11_467+19delinsTTGTGGAGA	XP_011520155.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521854.1:c.467+11_467+19delinsTTGTGGAGA	XP_011520156.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521855.1:c.467+11_467+19delinsTTGTGGAGA	XP_011520157.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521856.1:c.467+11_467+19delinsTTGTGGAGA	XP_011520158.1:n.467+11_467+19delinsTTGTGGAGA
XM_005254576.5:c.467+11_467+19delinsTTGTGGAGA	XP_005254633.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521855.3:c.467+11_467+19delinsTTGTGGAGA	XP_011520157.1:n.467+11_467+19delinsTTGTGGAGA
XM_011521856.2:c.467+11_467+19delinsTTGTGGAGA	XP_011520158.1:n.467+11_467+19delinsTTGTGGAGA
XM_024450009.1:c.467+11_467+19delinsTTGTGGAGA	XP_024305777.1:n.467+11_467+19delinsTTGTGGAGA
NM_183235.3:c.467+11_467+19delinsTTGTGGAGA MANE Select	NP_899058.1:n.467+11_467+19delinsTTGTGGAGA
NM_004580.5:c.467+11_467+19delinsTTGTGGAGA	NP_004571.2:n.467+11_467+19delinsTTGTGGAGA
NM_183236.3:c.467+11_467+19delinsTTGTGGAGA	NP_899059.1:n.467+11_467+19delinsTTGTGGAGA