Canonical Allele Identifier: CA1396548445

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs2080740848
• gnomAD v4: 3-119413830-ACAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413833_119413836del , CM000665.2:g.119413833_119413836del	GRCh38
NC_000003.11:g.119132680_119132683del , CM000665.1:g.119132680_119132683del	GRCh37
NC_000003.10:g.120615370_120615373del	NCBI36
NG_007665.2:g.124461_124464del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-23_1927-20del MANE Select	ENSP00000264245.4:n.1927-23_1927-20del
ENST00000264245.8:c.1927-23_1927-20del	ENSP00000264245.4:n.1927-23_1927-20del
NM_020754.3:c.1927-23_1927-20del	NP_065805.2:n.1927-23_1927-20del
XM_005247671.3:c.1834-23_1834-20del	XP_005247728.1:n.1834-23_1834-20del
XM_006713714.2:c.1867-23_1867-20del	XP_006713777.1:n.1867-23_1867-20del
XM_006713714.3:c.1867-23_1867-20del	XP_006713777.1:n.1867-23_1867-20del
XM_017006955.1:c.1435-23_1435-20del	XP_016862444.1:n.1435-23_1435-20del
NM_020754.4:c.1927-23_1927-20del MANE Select	NP_065805.2:n.1927-23_1927-20del