Canonical Allele Identifier: CA26863209

Gene: ARHGAP29

Linked Data

• dbSNP Id: rs142691086
• gnomAD v3: 1-94209083-T-G
• gnomAD v4: 1-94209083-T-G
• MyVariant Identifiers: chr1:g.94674639T>G (hg19) ; chr1:g.94209083T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209083T>G , CM000663.2:g.94209083T>G	GRCh38
NC_000001.10:g.94674639T>G , CM000663.1:g.94674639T>G	GRCh37
NC_000001.9:g.94447227T>G	NCBI36
NG_050965.1:g.70986A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260526.11:c.437+171A>C MANE Select	ENSP00000260526.6:n.437+171A>C
ENST00000260526.10:c.437+171A>C	ENSP00000260526.6:n.437+171A>C
ENST00000370217.3:c.437+171A>C	ENSP00000359237.3:n.437+171A>C
ENST00000552844.5:c.437+171A>C	ENSP00000449764.1:n.437+171A>C
NM_004815.3:c.437+171A>C	NP_004806.3:n.437+171A>C
XM_006711048.2:c.245+171A>C	XP_006711111.1:n.245+171A>C
XM_011542438.1:c.437+171A>C	XP_011540740.1:n.437+171A>C
XM_011542439.1:c.437+171A>C	XP_011540741.1:n.437+171A>C
XM_011542440.1:c.245+171A>C	XP_011540742.1:n.245+171A>C
NM_001328664.1:c.437+171A>C	NP_001315593.1:n.437+171A>C
NM_001328665.1:c.245+171A>C	NP_001315594.1:n.245+171A>C
NM_001328666.1:c.437+171A>C	NP_001315595.1:n.437+171A>C
NM_001328667.1:c.245+171A>C	NP_001315596.1:n.245+171A>C
XM_011542439.2:c.437+171A>C	XP_011540741.1:n.437+171A>C
NM_004815.4:c.437+171A>C MANE Select	NP_004806.3:n.437+171A>C
NM_001328664.2:c.437+171A>C	NP_001315593.1:n.437+171A>C
NM_001328665.2:c.245+171A>C	NP_001315594.1:n.245+171A>C
NM_001328666.2:c.437+171A>C	NP_001315595.1:n.437+171A>C
NM_001328667.2:c.245+171A>C	NP_001315596.1:n.245+171A>C