Canonical Allele Identifier: CA2760482982

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376764_13376766del , CM000666.2:g.13376764_13376766del	GRCh38
NC_000004.11:g.13378388_13378390del , CM000666.1:g.13378388_13378390del	GRCh37
NC_000004.10:g.12987486_12987488del	NCBI36
NG_033891.1:g.112601_112603del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-143_496-141del MANE Plus Clinical	ENSP00000288723.4:n.496-143_496-141del
ENST00000330852.10:c.496-143_496-141del MANE Select	ENSP00000328551.5:n.496-143_496-141del
ENST00000288723.8:c.496-143_496-141del	ENSP00000288723.4:n.496-143_496-141del
ENST00000330852.9:c.496-143_496-141del	ENSP00000328551.5:n.496-143_496-141del
ENST00000338176.8:c.496-143_496-141del	ENSP00000340079.4:n.496-143_496-141del
ENST00000504644.1:c.105-143_105-141del
ENST00000508274.5:c.*78-143_*78-141del	ENSP00000424043.1:n.*78-143_*78-141del
ENST00000511649.5:c.263-143_263-141del
ENST00000630951.1:c.*78-143_*78-141del	ENSP00000485808.1:n.*78-143_*78-141del
NM_001017979.2:c.496-143_496-141del	NP_001017979.1:n.496-143_496-141del
NM_001159601.1:c.496-143_496-141del	NP_001153073.1:n.496-143_496-141del
NM_004249.3:c.496-143_496-141del	NP_004240.2:n.496-143_496-141del
XM_005248215.3:c.496-143_496-141del	XP_005248272.1:n.496-143_496-141del
XM_011513911.1:c.496-143_496-141del	XP_011512213.1:n.496-143_496-141del
XM_011513912.1:c.265-143_265-141del	XP_011512214.1:n.265-143_265-141del
XR_925360.1:n.711-143_711-141del
XR_925361.1:n.711-143_711-141del
NM_001017979.3:c.496-143_496-141del MANE Select	NP_001017979.1:n.496-143_496-141del
NM_004249.4:c.496-143_496-141del MANE Plus Clinical	NP_004240.2:n.496-143_496-141del
NM_001159601.2:c.496-143_496-141del	NP_001153073.1:n.496-143_496-141del