Canonical Allele Identifier: CA1439616891

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376829A= , CM000666.2:g.13376829A=	GRCh38
NC_000004.11:g.13378453A= , CM000666.1:g.13378453A=	GRCh37
NC_000004.10:g.12987551A=	NCBI36
NG_033891.1:g.112537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-207T= MANE Plus Clinical	ENSP00000288723.4:n.496-207T=
ENST00000330852.10:c.496-207T= MANE Select	ENSP00000328551.5:n.496-207T=
ENST00000288723.8:c.496-207T=	ENSP00000288723.4:n.496-207T=
ENST00000330852.9:c.496-207T=	ENSP00000328551.5:n.496-207T=
ENST00000338176.8:c.496-207T=	ENSP00000340079.4:n.496-207T=
ENST00000504644.1:c.105-207T=
ENST00000508274.5:c.*78-207T=	ENSP00000424043.1:n.*78-207T=
ENST00000511649.5:c.263-207T=
ENST00000630951.1:c.*78-207T=	ENSP00000485808.1:n.*78-207T=
NM_001017979.2:c.496-207T=	NP_001017979.1:n.496-207T=
NM_001159601.1:c.496-207T=	NP_001153073.1:n.496-207T=
NM_004249.3:c.496-207T=	NP_004240.2:n.496-207T=
XM_005248215.3:c.496-207T=	XP_005248272.1:n.496-207T=
XM_011513911.1:c.496-207T=	XP_011512213.1:n.496-207T=
XM_011513912.1:c.265-207T=	XP_011512214.1:n.265-207T=
XR_925360.1:n.711-207T=
XR_925361.1:n.711-207T=
NM_001017979.3:c.496-207T= MANE Select	NP_001017979.1:n.496-207T=
NM_004249.4:c.496-207T= MANE Plus Clinical	NP_004240.2:n.496-207T=
NM_001159601.2:c.496-207T=	NP_001153073.1:n.496-207T=