Canonical Allele Identifier: CA1396548528

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414061_119414067delinsTCTCCAC , CM000665.2:g.119414061_119414067delinsTCTCCAC	GRCh38
NC_000003.11:g.119132908_119132914delinsTCTCCAC , CM000665.1:g.119132908_119132914delinsTCTCCAC	GRCh37
NC_000003.10:g.120615598_120615604delinsTCTCCAC	NCBI36
NG_007665.2:g.124689_124695delinsTCTCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2132_2138delinsTCTCCAC MANE Select	ENSP00000264245.4:p.Val711=
ENST00000264245.8:c.2132_2138delinsTCTCCAC	ENSP00000264245.4:p.Val711=
NM_020754.3:c.2132_2138delinsTCTCCAC	NP_065805.2:p.Val711=
XM_005247671.3:c.2039_2045delinsTCTCCAC	XP_005247728.1:p.Val680=
XM_006713714.2:c.2072_2078delinsTCTCCAC	XP_006713777.1:p.Val691=
XM_006713714.3:c.2072_2078delinsTCTCCAC	XP_006713777.1:p.Val691=
XM_017006955.1:c.1640_1646delinsTCTCCAC	XP_016862444.1:p.Val547=
NM_020754.4:c.2132_2138delinsTCTCCAC MANE Select	NP_065805.2:p.Val711=