Canonical Allele Identifier: CA1396548424

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413784_119413785delinsCT , CM000665.2:g.119413784_119413785delinsCT	GRCh38
NC_000003.11:g.119132631_119132632delinsCT , CM000665.1:g.119132631_119132632delinsCT	GRCh37
NC_000003.10:g.120615321_120615322delinsCT	NCBI36
NG_007665.2:g.124412_124413delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-72_1927-71delinsCT MANE Select	ENSP00000264245.4:n.1927-72_1927-71delinsCT
ENST00000264245.8:c.1927-72_1927-71delinsCT	ENSP00000264245.4:n.1927-72_1927-71delinsCT
NM_020754.3:c.1927-72_1927-71delinsCT	NP_065805.2:n.1927-72_1927-71delinsCT
XM_005247671.3:c.1834-72_1834-71delinsCT	XP_005247728.1:n.1834-72_1834-71delinsCT
XM_006713714.2:c.1867-72_1867-71delinsCT	XP_006713777.1:n.1867-72_1867-71delinsCT
XM_006713714.3:c.1867-72_1867-71delinsCT	XP_006713777.1:n.1867-72_1867-71delinsCT
XM_017006955.1:c.1435-72_1435-71delinsCT	XP_016862444.1:n.1435-72_1435-71delinsCT
NM_020754.4:c.1927-72_1927-71delinsCT MANE Select	NP_065805.2:n.1927-72_1927-71delinsCT