Canonical Allele Identifier: CA1439616860

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376741G= , CM000666.2:g.13376741G=	GRCh38
NC_000004.11:g.13378365G= , CM000666.1:g.13378365G=	GRCh37
NC_000004.10:g.12987463G=	NCBI36
NG_033891.1:g.112625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-119C= MANE Plus Clinical	ENSP00000288723.4:n.496-119C=
ENST00000330852.10:c.496-119C= MANE Select	ENSP00000328551.5:n.496-119C=
ENST00000288723.8:c.496-119C=	ENSP00000288723.4:n.496-119C=
ENST00000330852.9:c.496-119C=	ENSP00000328551.5:n.496-119C=
ENST00000338176.8:c.496-119C=	ENSP00000340079.4:n.496-119C=
ENST00000504644.1:c.105-119C=
ENST00000508274.5:c.*78-119C=	ENSP00000424043.1:n.*78-119C=
ENST00000511649.5:c.263-119C=
ENST00000630951.1:c.*78-119C=	ENSP00000485808.1:n.*78-119C=
NM_001017979.2:c.496-119C=	NP_001017979.1:n.496-119C=
NM_001159601.1:c.496-119C=	NP_001153073.1:n.496-119C=
NM_004249.3:c.496-119C=	NP_004240.2:n.496-119C=
XM_005248215.3:c.496-119C=	XP_005248272.1:n.496-119C=
XM_011513911.1:c.496-119C=	XP_011512213.1:n.496-119C=
XM_011513912.1:c.265-119C=	XP_011512214.1:n.265-119C=
XR_925360.1:n.711-119C=
XR_925361.1:n.711-119C=
NM_001017979.3:c.496-119C= MANE Select	NP_001017979.1:n.496-119C=
NM_004249.4:c.496-119C= MANE Plus Clinical	NP_004240.2:n.496-119C=
NM_001159601.2:c.496-119C=	NP_001153073.1:n.496-119C=