Canonical Allele Identifier: CA26863207

Gene: ARHGAP29

Linked Data

• dbSNP Id: rs567027636
• gnomAD v3: 1-94209079-G-C
• gnomAD v4: 1-94209079-G-C
• MyVariant Identifiers: chr1:g.94674635G>C (hg19) ; chr1:g.94209079G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209079G>C , CM000663.2:g.94209079G>C	GRCh38
NC_000001.10:g.94674635G>C , CM000663.1:g.94674635G>C	GRCh37
NC_000001.9:g.94447223G>C	NCBI36
NG_050965.1:g.70990C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260526.11:c.438-175C>G MANE Select	ENSP00000260526.6:n.438-175C>G
ENST00000260526.10:c.438-175C>G	ENSP00000260526.6:n.438-175C>G
ENST00000370217.3:c.438-175C>G	ENSP00000359237.3:n.438-175C>G
ENST00000552844.5:c.438-175C>G	ENSP00000449764.1:n.438-175C>G
NM_004815.3:c.438-175C>G	NP_004806.3:n.438-175C>G
XM_006711048.2:c.246-175C>G	XP_006711111.1:n.246-175C>G
XM_011542438.1:c.438-175C>G	XP_011540740.1:n.438-175C>G
XM_011542439.1:c.438-175C>G	XP_011540741.1:n.438-175C>G
XM_011542440.1:c.246-175C>G	XP_011540742.1:n.246-175C>G
NM_001328664.1:c.438-175C>G	NP_001315593.1:n.438-175C>G
NM_001328665.1:c.246-175C>G	NP_001315594.1:n.246-175C>G
NM_001328666.1:c.438-175C>G	NP_001315595.1:n.438-175C>G
NM_001328667.1:c.246-175C>G	NP_001315596.1:n.246-175C>G
XM_011542439.2:c.438-175C>G	XP_011540741.1:n.438-175C>G
NM_004815.4:c.438-175C>G MANE Select	NP_004806.3:n.438-175C>G
NM_001328664.2:c.438-175C>G	NP_001315593.1:n.438-175C>G
NM_001328665.2:c.246-175C>G	NP_001315594.1:n.246-175C>G
NM_001328666.2:c.438-175C>G	NP_001315595.1:n.438-175C>G
NM_001328667.2:c.246-175C>G	NP_001315596.1:n.246-175C>G