Canonical Allele Identifier: CA2178757188

Gene: RAB27A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55289044T= , CM000677.2:g.55289044T=	GRCh38
NC_000015.9:g.55581242T= , CM000677.1:g.55581242T=	GRCh37
NC_000015.8:g.53368534T=	NCBI36
NG_009103.1:g.5760A= , LRG_96:g.5760A=

Transcript Alleles

HGVS	Amino-acid Change
NM_183235.3:c.-143+672A= MANE Select	NP_899058.1:n.-143+672A=
ENST00000336787.6:c.-143+672A= MANE Select	ENSP00000337761.1:n.-143+672A=
NM_183235.2:c.-143+672A=	NP_899058.1:n.-143+672A=
ENST00000336787.5:c.-143+672A=	ENSP00000337761.1:n.-143+672A=
ENST00000563262.5:c.-112+24995A=	ENSP00000457595.1:n.-112+24995A=
ENST00000565776.1:n.76+672A=
ENST00000565776.2:n.76+672A=
ENST00000567639.1:n.98+672A=
ENST00000697642.1:c.-23+672A=	ENSP00000513368.1:n.-23+672A=
ENST00000697643.1:c.-232+672A=	ENSP00000513369.1:n.-232+672A=
XM_005254576.3:c.-23+672A=	XP_005254633.1:n.-23+672A=
XM_005254576.5:c.-23+672A=	XP_005254633.1:n.-23+672A=
XM_011521852.1:c.-359+672A=	XP_011520154.1:n.-359+672A=
XM_011521853.1:c.-462+672A=	XP_011520155.1:n.-462+672A=
XM_011521854.1:c.-232+672A=	XP_011520156.1:n.-232+672A=
XM_011521855.1:c.-246+672A=	XP_011520157.1:n.-246+672A=
XM_011521855.3:c.-246+672A=	XP_011520157.1:n.-246+672A=
XM_024450009.1:c.-462+672A=	XP_024305777.1:n.-462+672A=