Canonical Allele Identifier: CA2278712644

Gene: ARHGDIA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868844_81868848delinsCGTCA , CM000679.2:g.81868844_81868848delinsCGTCA	GRCh38
NC_000017.10:g.79826720_79826724delinsCGTCA , CM000679.1:g.79826720_79826724delinsCGTCA	GRCh37
NC_000017.9:g.77420009_77420013delinsCGTCA	NCBI36
NG_034210.1:g.7559_7563delinsTGACG

Transcript Alleles

HGVS	Amino-acid change
ENST00000269321.12:c.*28_*32delinsTGACG MANE Select	ENSP00000269321.7:n.*28_*32delinsTGACG
ENST00000269321.11:c.*28_*32delinsTGACG	ENSP00000269321.7:n.*28_*32delinsTGACG
ENST00000400721.8:c.*28_*32delinsTGACG	ENSP00000383556.4:n.*28_*32delinsTGACG
ENST00000541078.6:c.*28_*32delinsTGACG	ENSP00000441348.2:n.*28_*32delinsTGACG
ENST00000579121.5:c.502+141_502+145delinsTGACG	ENSP00000462960.1:n.502+141_502+145delinsTGACG
ENST00000580685.5:c.*28_*32delinsTGACG	ENSP00000464205.1:n.*28_*32delinsTGACG
ENST00000581876.5:c.*28_*32delinsTGACG	ENSP00000461956.1:n.*28_*32delinsTGACG
ENST00000583868.5:c.531_535delinsTGACG	ENSP00000462209.1:p.Thr177=
ENST00000584461.5:c.502+141_502+145delinsTGACG	ENSP00000463939.1:n.502+141_502+145delinsTGACG
NM_001185077.2:c.*28_*32delinsTGACG	NP_001172006.1:n.*28_*32delinsTGACG
NM_001185078.2:c.*28_*32delinsTGACG	NP_001172007.1:n.*28_*32delinsTGACG
NM_001301240.1:c.502+141_502+145delinsTGACG	NP_001288169.1:n.502+141_502+145delinsTGACG
NM_001301241.1:c.502+141_502+145delinsTGACG	NP_001288170.1:n.502+141_502+145delinsTGACG
NM_001301242.1:c.531_535delinsTGACG	NP_001288171.1:p.Thr177=
NM_001301243.1:c.*28_*32delinsTGACG	NP_001288172.1:n.*28_*32delinsTGACG
NM_004309.5:c.*28_*32delinsTGACG	NP_004300.1:n.*28_*32delinsTGACG
NR_125441.1:n.702_706delinsTGACG
XM_011523574.1:c.*28_*32delinsTGACG	XP_011521876.1:n.*28_*32delinsTGACG
NM_004309.6:c.*28_*32delinsTGACG MANE Select	NP_004300.1:n.*28_*32delinsTGACG
NM_001185077.3:c.*28_*32delinsTGACG	NP_001172006.1:n.*28_*32delinsTGACG
NM_001185078.3:c.*28_*32delinsTGACG	NP_001172007.1:n.*28_*32delinsTGACG
NM_001301240.2:c.502+141_502+145delinsTGACG	NP_001288169.1:n.502+141_502+145delinsTGACG
NM_001301241.2:c.502+141_502+145delinsTGACG	NP_001288170.1:n.502+141_502+145delinsTGACG
NM_001301242.2:c.531_535delinsTGACG	NP_001288171.1:p.Thr177=
NM_001301243.2:c.*28_*32delinsTGACG	NP_001288172.1:n.*28_*32delinsTGACG
NR_125441.2:n.633_637delinsTGACG