Canonical Allele Identifier: CA490429143

Gene: RAB27A

Linked Data

• MyVariant Identifiers: chr15:g.55516133T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55223935T>G , CM000677.2:g.55223935T>G	GRCh38
NC_000015.9:g.55516133T>G , CM000677.1:g.55516133T>G	GRCh37
NC_000015.8:g.53303425T>G	NCBI36
NG_009103.1:g.70869A>C , LRG_96:g.70869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697641.1:n.2457A>C
ENST00000697642.1:c.421A>C	ENSP00000513368.1:p.Arg141=
ENST00000697643.1:c.421A>C	ENSP00000513369.1:p.Arg141=
ENST00000697644.1:n.2589A>C
ENST00000336787.6:c.421A>C MANE Select	ENSP00000337761.1:p.Arg141=
ENST00000336787.5:c.421A>C	ENSP00000337761.1:p.Arg141=
ENST00000396307.6:c.421A>C	ENSP00000379601.2:p.Arg141=
ENST00000564609.5:c.421A>C	ENSP00000455012.1:p.Arg141=
ENST00000566877.5:c.421A>C	ENSP00000454695.1:p.Arg141=
ENST00000567380.5:c.421A>C	ENSP00000458127.1:p.Arg141=
ENST00000569493.5:c.421A>C	ENSP00000456059.1:p.Arg141=
NM_004580.4:c.421A>C	NP_004571.2:p.Arg141=
NM_183234.2:c.421A>C	NP_899057.1:p.Arg141=
NM_183235.2:c.421A>C	NP_899058.1:p.Arg141=
NM_183236.2:c.421A>C	NP_899059.1:p.Arg141=
XM_005254576.3:c.421A>C	XP_005254633.1:p.Arg141=
XM_011521852.1:c.421A>C	XP_011520154.1:p.Arg141=
XM_011521853.1:c.421A>C	XP_011520155.1:p.Arg141=
XM_011521854.1:c.421A>C	XP_011520156.1:p.Arg141=
XM_011521855.1:c.421A>C	XP_011520157.1:p.Arg141=
XM_011521856.1:c.421A>C	XP_011520158.1:p.Arg141=
XM_005254576.5:c.421A>C	XP_005254633.1:p.Arg141=
XM_011521855.3:c.421A>C	XP_011520157.1:p.Arg141=
XM_011521856.2:c.421A>C	XP_011520158.1:p.Arg141=
XM_024450009.1:c.421A>C	XP_024305777.1:p.Arg141=
NM_183235.3:c.421A>C MANE Select	NP_899058.1:p.Arg141=
NM_004580.5:c.421A>C	NP_004571.2:p.Arg141=
NM_183236.3:c.421A>C	NP_899059.1:p.Arg141=