Canonical Allele Identifier: CA401523287

Gene: ARHGDIA

Linked Data

• MyVariant Identifiers: chr17:g.79826771T>A (hg19) ; chr17:g.81868895T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81868895T>A , CM000679.2:g.81868895T>A	GRCh38
NC_000017.10:g.79826771T>A , CM000679.1:g.79826771T>A	GRCh37
NC_000017.9:g.77420060T>A	NCBI36
NG_034210.1:g.7512A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269321.12:c.596A>T MANE Select	ENSP00000269321.7:p.Lys199Met
ENST00000269321.11:c.596A>T	ENSP00000269321.7:p.Lys199Met
ENST00000400721.8:c.464A>T	ENSP00000383556.4:p.Lys155Met
ENST00000541078.6:c.596A>T	ENSP00000441348.2:p.Lys199Met
ENST00000579121.5:c.502+94A>T	ENSP00000462960.1:n.502+94A>T
ENST00000580685.5:c.596A>T	ENSP00000464205.1:p.Lys199Met
ENST00000581876.5:c.371A>T	ENSP00000461956.1:p.Lys124Met
ENST00000582984.5:n.798A>T
ENST00000583868.5:c.484A>T	ENSP00000462209.1:p.Arg162Ter
ENST00000584461.5:c.502+94A>T	ENSP00000463939.1:n.502+94A>T
NM_001185077.2:c.596A>T	NP_001172006.1:p.Lys199Met
NM_001185078.2:c.464A>T	NP_001172007.1:p.Lys155Met
NM_001301240.1:c.502+94A>T	NP_001288169.1:n.502+94A>T
NM_001301241.1:c.502+94A>T	NP_001288170.1:n.502+94A>T
NM_001301242.1:c.484A>T	NP_001288171.1:p.Arg162Ter
NM_001301243.1:c.731A>T	NP_001288172.1:p.Lys244Met
NM_004309.5:c.596A>T	NP_004300.1:p.Lys199Met
NR_125441.1:n.655A>T
XM_011523574.1:c.731A>T	XP_011521876.1:p.Lys244Met
NM_004309.6:c.596A>T MANE Select	NP_004300.1:p.Lys199Met
NM_001185077.3:c.596A>T	NP_001172006.1:p.Lys199Met
NM_001185078.3:c.464A>T	NP_001172007.1:p.Lys155Met
NM_001301240.2:c.502+94A>T	NP_001288169.1:n.502+94A>T
NM_001301241.2:c.502+94A>T	NP_001288170.1:n.502+94A>T
NM_001301242.2:c.484A>T	NP_001288171.1:p.Arg162Ter
NM_001301243.2:c.731A>T	NP_001288172.1:p.Lys244Met
NR_125441.2:n.586A>T