Canonical Allele Identifier: CA26863200

Gene: ARHGAP29

Linked Data

• dbSNP Id: rs181499128
• gnomAD v2: 1-94674628-C-T
• gnomAD v3: 1-94209072-C-T
• gnomAD v4: 1-94209072-C-T
• MyVariant Identifiers: chr1:g.94674628C>T (hg19) ; chr1:g.94209072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94209072C>T , CM000663.2:g.94209072C>T	GRCh38
NC_000001.10:g.94674628C>T , CM000663.1:g.94674628C>T	GRCh37
NC_000001.9:g.94447216C>T	NCBI36
NG_050965.1:g.70997G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260526.11:c.438-168G>A MANE Select	ENSP00000260526.6:n.438-168G>A
ENST00000260526.10:c.438-168G>A	ENSP00000260526.6:n.438-168G>A
ENST00000370217.3:c.438-168G>A	ENSP00000359237.3:n.438-168G>A
ENST00000552844.5:c.438-168G>A	ENSP00000449764.1:n.438-168G>A
NM_004815.3:c.438-168G>A	NP_004806.3:n.438-168G>A
XM_006711048.2:c.246-168G>A	XP_006711111.1:n.246-168G>A
XM_011542438.1:c.438-168G>A	XP_011540740.1:n.438-168G>A
XM_011542439.1:c.438-168G>A	XP_011540741.1:n.438-168G>A
XM_011542440.1:c.246-168G>A	XP_011540742.1:n.246-168G>A
NM_001328664.1:c.438-168G>A	NP_001315593.1:n.438-168G>A
NM_001328665.1:c.246-168G>A	NP_001315594.1:n.246-168G>A
NM_001328666.1:c.438-168G>A	NP_001315595.1:n.438-168G>A
NM_001328667.1:c.246-168G>A	NP_001315596.1:n.246-168G>A
XM_011542439.2:c.438-168G>A	XP_011540741.1:n.438-168G>A
NM_004815.4:c.438-168G>A MANE Select	NP_004806.3:n.438-168G>A
NM_001328664.2:c.438-168G>A	NP_001315593.1:n.438-168G>A
NM_001328665.2:c.246-168G>A	NP_001315594.1:n.246-168G>A
NM_001328666.2:c.438-168G>A	NP_001315595.1:n.438-168G>A
NM_001328667.2:c.246-168G>A	NP_001315596.1:n.246-168G>A