Canonical Allele Identifier: CA502425161

Gene: ARHGDIA

Linked Data

• dbSNP Id: rs1452644513
• gnomAD v2: 17-79826920-A-G
• gnomAD v3: 17-81869044-A-G
• gnomAD v4: 17-81869044-A-G
• MyVariant Identifiers: chr17:g.79826920A>G (hg19) ; chr17:g.81869044A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81869044A>G , CM000679.2:g.81869044A>G	GRCh38
NC_000017.10:g.79826920A>G , CM000679.1:g.79826920A>G	GRCh37
NC_000017.9:g.77420209A>G	NCBI36
NG_034210.1:g.7363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.447T>C MANE Select	ENSP00000269321.7:p.Tyr149=
ENST00000269321.11:c.447T>C	ENSP00000269321.7:p.Tyr149=
ENST00000400721.8:c.416-101T>C	ENSP00000383556.4:n.416-101T>C
ENST00000541078.6:c.447T>C	ENSP00000441348.2:p.Tyr149=
ENST00000579121.5:c.447T>C	ENSP00000462960.1:p.Tyr149=
ENST00000580033.5:c.*91T>C	ENSP00000463530.1:n.*91T>C
ENST00000580685.5:c.447T>C	ENSP00000464205.1:p.Tyr149=
ENST00000581876.5:c.222T>C	ENSP00000461956.1:p.Tyr74=
ENST00000582984.5:n.649T>C
ENST00000583791.1:n.311T>C
ENST00000583868.5:c.435+12T>C	ENSP00000462209.1:n.435+12T>C
ENST00000584461.5:c.447T>C	ENSP00000463939.1:p.Tyr149=
NM_001185077.2:c.447T>C	NP_001172006.1:p.Tyr149=
NM_001185078.2:c.416-101T>C	NP_001172007.1:n.416-101T>C
NM_001301240.1:c.447T>C	NP_001288169.1:p.Tyr149=
NM_001301241.1:c.447T>C	NP_001288170.1:p.Tyr149=
NM_001301242.1:c.435+12T>C	NP_001288171.1:n.435+12T>C
NM_001301243.1:c.582T>C	NP_001288172.1:p.Tyr194=
NM_004309.5:c.447T>C	NP_004300.1:p.Tyr149=
NR_125441.1:n.506T>C
XM_011523574.1:c.582T>C	XP_011521876.1:p.Tyr194=
NM_004309.6:c.447T>C MANE Select	NP_004300.1:p.Tyr149=
NM_001185077.3:c.447T>C	NP_001172006.1:p.Tyr149=
NM_001185078.3:c.416-101T>C	NP_001172007.1:n.416-101T>C
NM_001301240.2:c.447T>C	NP_001288169.1:p.Tyr149=
NM_001301241.2:c.447T>C	NP_001288170.1:p.Tyr149=
NM_001301242.2:c.435+12T>C	NP_001288171.1:n.435+12T>C
NM_001301243.2:c.582T>C	NP_001288172.1:p.Tyr194=
NR_125441.2:n.437T>C