Canonical Allele Identifier: CA81697371

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs34914603
• MyVariant Identifiers: chr3:g.119132843_119132844insG (hg19) ; chr3:g.119413996_119413997insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413996_119413997insG , CM000665.2:g.119413996_119413997insG	GRCh38
NC_000003.11:g.119132843_119132844insG , CM000665.1:g.119132843_119132844insG	GRCh37
NC_000003.10:g.120615533_120615534insG	NCBI36
NG_007665.2:g.124624_124625insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2067_2068insG MANE Select	ENSP00000264245.4:p.Leu690AlafsTer?
ENST00000264245.8:c.2067_2068insG	ENSP00000264245.4:p.Leu690AlafsTer?
NM_020754.3:c.2067_2068insG	NP_065805.2:p.Leu690AlafsTer?
XM_005247671.3:c.1974_1975insG	XP_005247728.1:p.Leu659AlafsTer?
XM_006713714.2:c.2007_2008insG	XP_006713777.1:p.Leu670AlafsTer?
XM_006713714.3:c.2007_2008insG	XP_006713777.1:p.Leu670AlafsTer?
XM_017006955.1:c.1575_1576insG	XP_016862444.1:p.Leu526AlafsTer?
NM_020754.4:c.2067_2068insG MANE Select	NP_065805.2:p.Leu690AlafsTer?