Canonical Allele Identifier: CA2760482989

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376766_13376767insAC , CM000666.2:g.13376766_13376767insAC	GRCh38
NC_000004.11:g.13378390_13378391insAC , CM000666.1:g.13378390_13378391insAC	GRCh37
NC_000004.10:g.12987488_12987489insAC	NCBI36
NG_033891.1:g.112599_112600insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-145_496-144insGT MANE Plus Clinical	ENSP00000288723.4:n.496-145_496-144insGT
ENST00000330852.10:c.496-145_496-144insGT MANE Select	ENSP00000328551.5:n.496-145_496-144insGT
ENST00000288723.8:c.496-145_496-144insGT	ENSP00000288723.4:n.496-145_496-144insGT
ENST00000330852.9:c.496-145_496-144insGT	ENSP00000328551.5:n.496-145_496-144insGT
ENST00000338176.8:c.496-145_496-144insGT	ENSP00000340079.4:n.496-145_496-144insGT
ENST00000504644.1:c.105-145_105-144insGT
ENST00000508274.5:c.*78-145_*78-144insGT	ENSP00000424043.1:n.*78-145_*78-144insGT
ENST00000511649.5:c.263-145_263-144insGT
ENST00000630951.1:c.*78-145_*78-144insGT	ENSP00000485808.1:n.*78-145_*78-144insGT
NM_001017979.2:c.496-145_496-144insGT	NP_001017979.1:n.496-145_496-144insGT
NM_001159601.1:c.496-145_496-144insGT	NP_001153073.1:n.496-145_496-144insGT
NM_004249.3:c.496-145_496-144insGT	NP_004240.2:n.496-145_496-144insGT
XM_005248215.3:c.496-145_496-144insGT	XP_005248272.1:n.496-145_496-144insGT
XM_011513911.1:c.496-145_496-144insGT	XP_011512213.1:n.496-145_496-144insGT
XM_011513912.1:c.265-145_265-144insGT	XP_011512214.1:n.265-145_265-144insGT
XR_925360.1:n.711-145_711-144insGT
XR_925361.1:n.711-145_711-144insGT
NM_001017979.3:c.496-145_496-144insGT MANE Select	NP_001017979.1:n.496-145_496-144insGT
NM_004249.4:c.496-145_496-144insGT MANE Plus Clinical	NP_004240.2:n.496-145_496-144insGT
NM_001159601.2:c.496-145_496-144insGT	NP_001153073.1:n.496-145_496-144insGT