Canonical Allele Identifier: CA502425153

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826914G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869038G>C , CM000679.2:g.81869038G>C	GRCh38
NC_000017.10:g.79826914G>C , CM000679.1:g.79826914G>C	GRCh37
NC_000017.9:g.77420203G>C	NCBI36
NG_034210.1:g.7369C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.453C>G MANE Select	ENSP00000269321.7:p.Pro151=
ENST00000269321.11:c.453C>G	ENSP00000269321.7:p.Pro151=
ENST00000400721.8:c.416-95C>G	ENSP00000383556.4:n.416-95C>G
ENST00000541078.6:c.453C>G	ENSP00000441348.2:p.Pro151=
ENST00000579121.5:c.453C>G	ENSP00000462960.1:p.Pro151=
ENST00000580033.5:c.*97C>G	ENSP00000463530.1:n.*97C>G
ENST00000580685.5:c.453C>G	ENSP00000464205.1:p.Pro151=
ENST00000581876.5:c.228C>G	ENSP00000461956.1:p.Pro76=
ENST00000582984.5:n.655C>G
ENST00000583791.1:n.317C>G
ENST00000583868.5:c.435+18C>G	ENSP00000462209.1:n.435+18C>G
ENST00000584461.5:c.453C>G	ENSP00000463939.1:p.Pro151=
NM_001185077.2:c.453C>G	NP_001172006.1:p.Pro151=
NM_001185078.2:c.416-95C>G	NP_001172007.1:n.416-95C>G
NM_001301240.1:c.453C>G	NP_001288169.1:p.Pro151=
NM_001301241.1:c.453C>G	NP_001288170.1:p.Pro151=
NM_001301242.1:c.435+18C>G	NP_001288171.1:n.435+18C>G
NM_001301243.1:c.588C>G	NP_001288172.1:p.Pro196=
NM_004309.5:c.453C>G	NP_004300.1:p.Pro151=
NR_125441.1:n.512C>G
XM_011523574.1:c.588C>G	XP_011521876.1:p.Pro196=
NM_004309.6:c.453C>G MANE Select	NP_004300.1:p.Pro151=
NM_001185077.3:c.453C>G	NP_001172006.1:p.Pro151=
NM_001185078.3:c.416-95C>G	NP_001172007.1:n.416-95C>G
NM_001301240.2:c.453C>G	NP_001288169.1:p.Pro151=
NM_001301241.2:c.453C>G	NP_001288170.1:p.Pro151=
NM_001301242.2:c.435+18C>G	NP_001288171.1:n.435+18C>G
NM_001301243.2:c.588C>G	NP_001288172.1:p.Pro196=
NR_125441.2:n.443C>G