Canonical Allele Identifier: CA401523205
Gene: ARHGDIA HGNC NCBI

Linked Data

dbSNP Id: rs1273198442

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81868884T>C , CM000679.2:g.81868884T>C GRCh38
NC_000017.10:g.79826760T>C , CM000679.1:g.79826760T>C GRCh37
NC_000017.9:g.77420049T>C NCBI36
NG_034210.1:g.7523A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269321.12:c.607A>G MANE Select ENSP00000269321.7:p.Lys203Glu
ENST00000269321.11:c.607A>G ENSP00000269321.7:p.Lys203Glu
ENST00000400721.8:c.475A>G ENSP00000383556.4:p.Lys159Glu
ENST00000541078.6:c.607A>G ENSP00000441348.2:p.Lys203Glu
ENST00000579121.5:c.502+105A>G ENSP00000462960.1:n.502+105A>G
ENST00000580685.5:c.607A>G ENSP00000464205.1:p.Lys203Glu
ENST00000581876.5:c.382A>G ENSP00000461956.1:p.Lys128Glu
ENST00000582984.5:n.809A>G
ENST00000583868.5:c.495A>G ENSP00000462209.1:p.Gly165=
ENST00000584461.5:c.502+105A>G ENSP00000463939.1:n.502+105A>G
NM_001185077.2:c.607A>G NP_001172006.1:p.Lys203Glu
NM_001185078.2:c.475A>G NP_001172007.1:p.Lys159Glu
NM_001301240.1:c.502+105A>G NP_001288169.1:n.502+105A>G
NM_001301241.1:c.502+105A>G NP_001288170.1:n.502+105A>G
NM_001301242.1:c.495A>G NP_001288171.1:p.Gly165=
NM_001301243.1:c.742A>G NP_001288172.1:p.Lys248Glu
NM_004309.5:c.607A>G NP_004300.1:p.Lys203Glu
NR_125441.1:n.666A>G
XM_011523574.1:c.742A>G XP_011521876.1:p.Lys248Glu
NM_004309.6:c.607A>G MANE Select NP_004300.1:p.Lys203Glu
NM_001185077.3:c.607A>G NP_001172006.1:p.Lys203Glu
NM_001185078.3:c.475A>G NP_001172007.1:p.Lys159Glu
NM_001301240.2:c.502+105A>G NP_001288169.1:n.502+105A>G
NM_001301241.2:c.502+105A>G NP_001288170.1:n.502+105A>G
NM_001301242.2:c.495A>G NP_001288171.1:p.Gly165=
NM_001301243.2:c.742A>G NP_001288172.1:p.Lys248Glu
NR_125441.2:n.597A>G