Canonical Allele Identifier: CA2278712810
Gene: ARHGDIA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81869141_81869142delinsGC , CM000679.2:g.81869141_81869142delinsGC GRCh38
NC_000017.10:g.79827017_79827018delinsGC , CM000679.1:g.79827017_79827018delinsGC GRCh37
NC_000017.9:g.77420306_77420307delinsGC NCBI36
NG_034210.1:g.7265_7266delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000269321.12:c.415+31_415+32delinsGC MANE Select ENSP00000269321.7:n.415+31_415+32delinsGC...
ENST00000269321.11:c.415+31_415+32delinsGC ENSP00000269321.7:n.415+31_415+32delinsGC...
ENST00000400721.8:c.415+31_415+32delinsGC ENSP00000383556.4:n.415+31_415+32delinsGC...
ENST00000541078.6:c.415+31_415+32delinsGC ENSP00000441348.2:n.415+31_415+32delinsGC...
ENST00000578351.1:c.*59+31_*59+32delinsGC ENSP00000462323.1:n.*59+31_*59+32delinsGC...
ENST00000579121.5:c.415+31_415+32delinsGC ENSP00000462960.1:n.415+31_415+32delinsGC...
ENST00000580033.5:c.*59+31_*59+32delinsGC ENSP00000463530.1:n.*59+31_*59+32delinsGC...
ENST00000580685.5:c.415+31_415+32delinsGC ENSP00000464205.1:n.415+31_415+32delinsGC...
ENST00000581876.5:c.191-67_191-66delinsGC ENSP00000461956.1:n.191-67_191-66delinsGC...
ENST00000582984.5:n.617+31_617+32delinsGC
ENST00000583791.1:n.279+31_279+32delinsGC
ENST00000583868.5:c.415+31_415+32delinsGC ENSP00000462209.1:n.415+31_415+32delinsGC...
ENST00000584461.5:c.415+31_415+32delinsGC ENSP00000463939.1:n.415+31_415+32delinsGC...
NM_001185077.2:c.415+31_415+32delinsGC NP_001172006.1:n.415+31_415+32delinsGC
NM_001185078.2:c.415+31_415+32delinsGC NP_001172007.1:n.415+31_415+32delinsGC
NM_001301240.1:c.415+31_415+32delinsGC NP_001288169.1:n.415+31_415+32delinsGC
NM_001301241.1:c.415+31_415+32delinsGC NP_001288170.1:n.415+31_415+32delinsGC
NM_001301242.1:c.415+31_415+32delinsGC NP_001288171.1:n.415+31_415+32delinsGC
NM_001301243.1:c.550+31_550+32delinsGC NP_001288172.1:n.550+31_550+32delinsGC
NM_004309.5:c.415+31_415+32delinsGC NP_004300.1:n.415+31_415+32delinsGC
NR_125441.1:n.474+31_474+32delinsGC
XM_011523574.1:c.550+31_550+32delinsGC XP_011521876.1:n.550+31_550+32delinsGC
NM_004309.6:c.415+31_415+32delinsGC MANE Select NP_004300.1:n.415+31_415+32delinsGC
NM_001185077.3:c.415+31_415+32delinsGC NP_001172006.1:n.415+31_415+32delinsGC
NM_001185078.3:c.415+31_415+32delinsGC NP_001172007.1:n.415+31_415+32delinsGC
NM_001301240.2:c.415+31_415+32delinsGC NP_001288169.1:n.415+31_415+32delinsGC
NM_001301241.2:c.415+31_415+32delinsGC NP_001288170.1:n.415+31_415+32delinsGC
NM_001301242.2:c.415+31_415+32delinsGC NP_001288171.1:n.415+31_415+32delinsGC
NM_001301243.2:c.550+31_550+32delinsGC NP_001288172.1:n.550+31_550+32delinsGC
NR_125441.2:n.405+31_405+32delinsGC