Canonical Allele Identifier: CA1439616869

Gene: RAB28

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13376757_13376761delinsCTTTA , CM000666.2:g.13376757_13376761delinsCTTTA	GRCh38
NC_000004.11:g.13378381_13378385delinsCTTTA , CM000666.1:g.13378381_13378385delinsCTTTA	GRCh37
NC_000004.10:g.12987479_12987483delinsCTTTA	NCBI36
NG_033891.1:g.112605_112609delinsTAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288723.9:c.496-139_496-135delinsTAAAG MANE Plus Clinical	ENSP00000288723.4:n.496-139_496-135delinsTAAAG
ENST00000330852.10:c.496-139_496-135delinsTAAAG MANE Select	ENSP00000328551.5:n.496-139_496-135delinsTAAAG
ENST00000288723.8:c.496-139_496-135delinsTAAAG	ENSP00000288723.4:n.496-139_496-135delinsTAAAG
ENST00000330852.9:c.496-139_496-135delinsTAAAG	ENSP00000328551.5:n.496-139_496-135delinsTAAAG
ENST00000338176.8:c.496-139_496-135delinsTAAAG	ENSP00000340079.4:n.496-139_496-135delinsTAAAG
ENST00000504644.1:c.105-139_105-135delinsTAAAG
ENST00000508274.5:c.*78-139_*78-135delinsTAAAG	ENSP00000424043.1:n.*78-139_*78-135delinsTAAAG
ENST00000511649.5:c.263-139_263-135delinsTAAAG
ENST00000630951.1:c.*78-139_*78-135delinsTAAAG	ENSP00000485808.1:n.*78-139_*78-135delinsTAAAG
NM_001017979.2:c.496-139_496-135delinsTAAAG	NP_001017979.1:n.496-139_496-135delinsTAAAG
NM_001159601.1:c.496-139_496-135delinsTAAAG	NP_001153073.1:n.496-139_496-135delinsTAAAG
NM_004249.3:c.496-139_496-135delinsTAAAG	NP_004240.2:n.496-139_496-135delinsTAAAG
XM_005248215.3:c.496-139_496-135delinsTAAAG	XP_005248272.1:n.496-139_496-135delinsTAAAG
XM_011513911.1:c.496-139_496-135delinsTAAAG	XP_011512213.1:n.496-139_496-135delinsTAAAG
XM_011513912.1:c.265-139_265-135delinsTAAAG	XP_011512214.1:n.265-139_265-135delinsTAAAG
XR_925360.1:n.711-139_711-135delinsTAAAG
XR_925361.1:n.711-139_711-135delinsTAAAG
NM_001017979.3:c.496-139_496-135delinsTAAAG MANE Select	NP_001017979.1:n.496-139_496-135delinsTAAAG
NM_004249.4:c.496-139_496-135delinsTAAAG MANE Plus Clinical	NP_004240.2:n.496-139_496-135delinsTAAAG
NM_001159601.2:c.496-139_496-135delinsTAAAG	NP_001153073.1:n.496-139_496-135delinsTAAAG