Canonical Allele Identifier: CA2640521812
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868657_81868671del , CM000679.2:g.81868657_81868671del GRCh38
NC_000017.10:g.79826533_79826547del , CM000679.1:g.79826533_79826547del GRCh37
NC_000017.9:g.77419822_77419836del NCBI36
NG_034210.1:g.7736_7750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.*205_*219del MANE Select ENSP00000269321.7:n.*205_*219del
ENST00000269321.11:c.*205_*219del ENSP00000269321.7:n.*205_*219del
ENST00000400721.8:c.*205_*219del ENSP00000383556.4:n.*205_*219del
ENST00000541078.6:c.*205_*219del ENSP00000441348.2:n.*205_*219del
ENST00000579121.5:c.503-87_503-73del ENSP00000462960.1:n.503-87_503-73del
ENST00000580685.5:c.*205_*219del ENSP00000464205.1:n.*205_*219del
ENST00000581876.5:c.*205_*219del ENSP00000461956.1:n.*205_*219del
ENST00000583868.5:c.708_722del ENSP00000462209.1:p.Val237_Val241del
ENST00000584461.5:c.503-87_503-73del ENSP00000463939.1:n.503-87_503-73del
NM_001185077.2:c.*205_*219del NP_001172006.1:n.*205_*219del
NM_001185078.2:c.*205_*219del NP_001172007.1:n.*205_*219del
NM_001301240.1:c.503-87_503-73del NP_001288169.1:n.503-87_503-73del
NM_001301241.1:c.503-87_503-73del NP_001288170.1:n.503-87_503-73del
NM_001301242.1:c.708_722del NP_001288171.1:p.Val237_Val241del
NM_001301243.1:c.*205_*219del NP_001288172.1:n.*205_*219del
NM_004309.5:c.*205_*219del NP_004300.1:n.*205_*219del
NR_125441.1:n.879_893del
XM_011523574.1:c.*205_*219del XP_011521876.1:n.*205_*219del
NM_004309.6:c.*205_*219del MANE Select NP_004300.1:n.*205_*219del
NM_001185077.3:c.*205_*219del NP_001172006.1:n.*205_*219del
NM_001185078.3:c.*205_*219del NP_001172007.1:n.*205_*219del
NM_001301240.2:c.503-87_503-73del NP_001288169.1:n.503-87_503-73del
NM_001301241.2:c.503-87_503-73del NP_001288170.1:n.503-87_503-73del
NM_001301242.2:c.708_722del NP_001288171.1:p.Val237_Val241del
NM_001301243.2:c.*205_*219del NP_001288172.1:n.*205_*219del
NR_125441.2:n.810_824del