Canonical Allele Identifier: CA502425132

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826881C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869005C>G , CM000679.2:g.81869005C>G	GRCh38
NC_000017.10:g.79826881C>G , CM000679.1:g.79826881C>G	GRCh37
NC_000017.9:g.77420170C>G	NCBI36
NG_034210.1:g.7402G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.486G>C MANE Select	ENSP00000269321.7:p.Val162=
ENST00000269321.11:c.486G>C	ENSP00000269321.7:p.Val162=
ENST00000400721.8:c.416-62G>C	ENSP00000383556.4:n.416-62G>C
ENST00000541078.6:c.486G>C	ENSP00000441348.2:p.Val162=
ENST00000579121.5:c.486G>C	ENSP00000462960.1:p.Val162=
ENST00000580033.5:c.*130G>C	ENSP00000463530.1:n.*130G>C
ENST00000580685.5:c.486G>C	ENSP00000464205.1:p.Val162=
ENST00000581876.5:c.261G>C	ENSP00000461956.1:p.Val87=
ENST00000582984.5:n.688G>C
ENST00000583791.1:n.350G>C
ENST00000583868.5:c.435+51G>C	ENSP00000462209.1:n.435+51G>C
ENST00000584461.5:c.486G>C	ENSP00000463939.1:p.Val162=
NM_001185077.2:c.486G>C	NP_001172006.1:p.Val162=
NM_001185078.2:c.416-62G>C	NP_001172007.1:n.416-62G>C
NM_001301240.1:c.486G>C	NP_001288169.1:p.Val162=
NM_001301241.1:c.486G>C	NP_001288170.1:p.Val162=
NM_001301242.1:c.435+51G>C	NP_001288171.1:n.435+51G>C
NM_001301243.1:c.621G>C	NP_001288172.1:p.Val207=
NM_004309.5:c.486G>C	NP_004300.1:p.Val162=
NR_125441.1:n.545G>C
XM_011523574.1:c.621G>C	XP_011521876.1:p.Val207=
NM_004309.6:c.486G>C MANE Select	NP_004300.1:p.Val162=
NM_001185077.3:c.486G>C	NP_001172006.1:p.Val162=
NM_001185078.3:c.416-62G>C	NP_001172007.1:n.416-62G>C
NM_001301240.2:c.486G>C	NP_001288169.1:p.Val162=
NM_001301241.2:c.486G>C	NP_001288170.1:p.Val162=
NM_001301242.2:c.435+51G>C	NP_001288171.1:n.435+51G>C
NM_001301243.2:c.621G>C	NP_001288172.1:p.Val207=
NR_125441.2:n.476G>C