Canonical Allele Identifier: CA401523470

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826796A>G (hg19) ; chr17:g.81868920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868920A>G , CM000679.2:g.81868920A>G	GRCh38
NC_000017.10:g.79826796A>G , CM000679.1:g.79826796A>G	GRCh37
NC_000017.9:g.77420085A>G	NCBI36
NG_034210.1:g.7487T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.571T>C MANE Select	ENSP00000269321.7:p.Ser191Pro
ENST00000269321.11:c.571T>C	ENSP00000269321.7:p.Ser191Pro
ENST00000400721.8:c.439T>C	ENSP00000383556.4:p.Ser147Pro
ENST00000541078.6:c.571T>C	ENSP00000441348.2:p.Ser191Pro
ENST00000579121.5:c.502+69T>C	ENSP00000462960.1:n.502+69T>C
ENST00000580685.5:c.571T>C	ENSP00000464205.1:p.Ser191Pro
ENST00000581876.5:c.346T>C	ENSP00000461956.1:p.Ser116Pro
ENST00000582984.5:n.773T>C
ENST00000583868.5:c.459T>C	ENSP00000462209.1:p.Cys153=
ENST00000584461.5:c.502+69T>C	ENSP00000463939.1:n.502+69T>C
NM_001185077.2:c.571T>C	NP_001172006.1:p.Ser191Pro
NM_001185078.2:c.439T>C	NP_001172007.1:p.Ser147Pro
NM_001301240.1:c.502+69T>C	NP_001288169.1:n.502+69T>C
NM_001301241.1:c.502+69T>C	NP_001288170.1:n.502+69T>C
NM_001301242.1:c.459T>C	NP_001288171.1:p.Cys153=
NM_001301243.1:c.706T>C	NP_001288172.1:p.Ser236Pro
NM_004309.5:c.571T>C	NP_004300.1:p.Ser191Pro
NR_125441.1:n.630T>C
XM_011523574.1:c.706T>C	XP_011521876.1:p.Ser236Pro
NM_004309.6:c.571T>C MANE Select	NP_004300.1:p.Ser191Pro
NM_001185077.3:c.571T>C	NP_001172006.1:p.Ser191Pro
NM_001185078.3:c.439T>C	NP_001172007.1:p.Ser147Pro
NM_001301240.2:c.502+69T>C	NP_001288169.1:n.502+69T>C
NM_001301241.2:c.502+69T>C	NP_001288170.1:n.502+69T>C
NM_001301242.2:c.459T>C	NP_001288171.1:p.Cys153=
NM_001301243.2:c.706T>C	NP_001288172.1:p.Ser236Pro
NR_125441.2:n.561T>C