Canonical Allele Identifier: CA401523877
Gene: ARHGDIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868992T>C , CM000679.2:g.81868992T>C GRCh38
NC_000017.10:g.79826868T>C , CM000679.1:g.79826868T>C GRCh37
NC_000017.9:g.77420157T>C NCBI36
NG_034210.1:g.7415A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.499A>G MANE Select ENSP00000269321.7:p.Lys167Glu
ENST00000269321.11:c.499A>G ENSP00000269321.7:p.Lys167Glu
ENST00000400721.8:c.416-49A>G ENSP00000383556.4:n.416-49A>G
ENST00000541078.6:c.499A>G ENSP00000441348.2:p.Lys167Glu
ENST00000579121.5:c.499A>G ENSP00000462960.1:p.Lys167Glu
ENST00000580033.5:c.*143A>G ENSP00000463530.1:n.*143A>G
ENST00000580685.5:c.499A>G ENSP00000464205.1:p.Lys167Glu
ENST00000581876.5:c.274A>G ENSP00000461956.1:p.Lys92Glu
ENST00000582984.5:n.701A>G
ENST00000583868.5:c.436-49A>G ENSP00000462209.1:n.436-49A>G
ENST00000584461.5:c.499A>G ENSP00000463939.1:p.Lys167Glu
NM_001185077.2:c.499A>G NP_001172006.1:p.Lys167Glu
NM_001185078.2:c.416-49A>G NP_001172007.1:n.416-49A>G
NM_001301240.1:c.499A>G NP_001288169.1:p.Lys167Glu
NM_001301241.1:c.499A>G NP_001288170.1:p.Lys167Glu
NM_001301242.1:c.436-49A>G NP_001288171.1:n.436-49A>G
NM_001301243.1:c.634A>G NP_001288172.1:p.Lys212Glu
NM_004309.5:c.499A>G NP_004300.1:p.Lys167Glu
NR_125441.1:n.558A>G
XM_011523574.1:c.634A>G XP_011521876.1:p.Lys212Glu
NM_004309.6:c.499A>G MANE Select NP_004300.1:p.Lys167Glu
NM_001185077.3:c.499A>G NP_001172006.1:p.Lys167Glu
NM_001185078.3:c.416-49A>G NP_001172007.1:n.416-49A>G
NM_001301240.2:c.499A>G NP_001288169.1:p.Lys167Glu
NM_001301241.2:c.499A>G NP_001288170.1:p.Lys167Glu
NM_001301242.2:c.436-49A>G NP_001288171.1:n.436-49A>G
NM_001301243.2:c.634A>G NP_001288172.1:p.Lys212Glu
NR_125441.2:n.489A>G