Canonical Allele Identifier: CA2760483016

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376801A>T , CM000666.2:g.13376801A>T	GRCh38
NC_000004.11:g.13378425A>T , CM000666.1:g.13378425A>T	GRCh37
NC_000004.10:g.12987523A>T	NCBI36
NG_033891.1:g.112565T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-179T>A MANE Plus Clinical	ENSP00000288723.4:n.496-179T>A
ENST00000330852.10:c.496-179T>A MANE Select	ENSP00000328551.5:n.496-179T>A
ENST00000288723.8:c.496-179T>A	ENSP00000288723.4:n.496-179T>A
ENST00000330852.9:c.496-179T>A	ENSP00000328551.5:n.496-179T>A
ENST00000338176.8:c.496-179T>A	ENSP00000340079.4:n.496-179T>A
ENST00000504644.1:c.105-179T>A
ENST00000508274.5:c.*78-179T>A	ENSP00000424043.1:n.*78-179T>A
ENST00000511649.5:c.263-179T>A
ENST00000630951.1:c.*78-179T>A	ENSP00000485808.1:n.*78-179T>A
NM_001017979.2:c.496-179T>A	NP_001017979.1:n.496-179T>A
NM_001159601.1:c.496-179T>A	NP_001153073.1:n.496-179T>A
NM_004249.3:c.496-179T>A	NP_004240.2:n.496-179T>A
XM_005248215.3:c.496-179T>A	XP_005248272.1:n.496-179T>A
XM_011513911.1:c.496-179T>A	XP_011512213.1:n.496-179T>A
XM_011513912.1:c.265-179T>A	XP_011512214.1:n.265-179T>A
XR_925360.1:n.711-179T>A
XR_925361.1:n.711-179T>A
NM_001017979.3:c.496-179T>A MANE Select	NP_001017979.1:n.496-179T>A
NM_004249.4:c.496-179T>A MANE Plus Clinical	NP_004240.2:n.496-179T>A
NM_001159601.2:c.496-179T>A	NP_001153073.1:n.496-179T>A