Canonical Allele Identifier: CA435412064

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133203A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414356A>G , CM000665.2:g.119414356A>G	GRCh38
NC_000003.11:g.119133203A>G , CM000665.1:g.119133203A>G	GRCh37
NC_000003.10:g.120615893A>G	NCBI36
NG_007665.2:g.124984A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2427A>G MANE Select	ENSP00000264245.4:p.Ser809=
ENST00000264245.8:c.2427A>G	ENSP00000264245.4:p.Ser809=
NM_020754.3:c.2427A>G	NP_065805.2:p.Ser809=
XM_005247671.3:c.2334A>G	XP_005247728.1:p.Ser778=
XM_006713714.2:c.2367A>G	XP_006713777.1:p.Ser789=
XM_006713714.3:c.2367A>G	XP_006713777.1:p.Ser789=
XM_017006955.1:c.1935A>G	XP_016862444.1:p.Ser645=
NM_020754.4:c.2427A>G MANE Select	NP_065805.2:p.Ser809=