Canonical Allele Identifier: CA2667110218

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413736-C-CATTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413736_119413737insATTAAAAAA , CM000665.2:g.119413736_119413737insATTAAAAAA	GRCh38
NC_000003.11:g.119132583_119132584insATTAAAAAA , CM000665.1:g.119132583_119132584insATTAAAAAA	GRCh37
NC_000003.10:g.120615273_120615274insATTAAAAAA	NCBI36
NG_007665.2:g.124364_124365insATTAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-120_1927-119insATTAAAAAA MANE Select	ENSP00000264245.4:n.1927-120_1927-119insATTAAAAAA
ENST00000264245.8:c.1927-120_1927-119insATTAAAAAA	ENSP00000264245.4:n.1927-120_1927-119insATTAAAAAA
NM_020754.3:c.1927-120_1927-119insATTAAAAAA	NP_065805.2:n.1927-120_1927-119insATTAAAAAA
XM_005247671.3:c.1834-120_1834-119insATTAAAAAA	XP_005247728.1:n.1834-120_1834-119insATTAAAAAA
XM_006713714.2:c.1867-120_1867-119insATTAAAAAA	XP_006713777.1:n.1867-120_1867-119insATTAAAAAA
XM_006713714.3:c.1867-120_1867-119insATTAAAAAA	XP_006713777.1:n.1867-120_1867-119insATTAAAAAA
XM_017006955.1:c.1435-120_1435-119insATTAAAAAA	XP_016862444.1:n.1435-120_1435-119insATTAAAAAA
NM_020754.4:c.1927-120_1927-119insATTAAAAAA MANE Select	NP_065805.2:n.1927-120_1927-119insATTAAAAAA