Canonical Allele Identifier: CA897778704

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1222808162
• gnomAD v3: 3-119413468-TTTG-T
• gnomAD v4: 3-119413468-TTTG-T
• MyVariant Identifiers: chr3:g.119132316_119132318del (hg19) ; chr3:g.119413469_119413471del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413474_119413476del , CM000665.2:g.119413474_119413476del	GRCh38
NC_000003.11:g.119132321_119132323del , CM000665.1:g.119132321_119132323del	GRCh37
NC_000003.10:g.120615011_120615013del	NCBI36
NG_007665.2:g.124102_124104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-382_1927-380del MANE Select	ENSP00000264245.4:n.1927-382_1927-380del
ENST00000264245.8:c.1927-382_1927-380del	ENSP00000264245.4:n.1927-382_1927-380del
NM_020754.3:c.1927-382_1927-380del	NP_065805.2:n.1927-382_1927-380del
XM_005247671.3:c.1834-382_1834-380del	XP_005247728.1:n.1834-382_1834-380del
XM_006713714.2:c.1867-382_1867-380del	XP_006713777.1:n.1867-382_1867-380del
XM_006713714.3:c.1867-382_1867-380del	XP_006713777.1:n.1867-382_1867-380del
XM_017006955.1:c.1435-382_1435-380del	XP_016862444.1:n.1435-382_1435-380del
NM_020754.4:c.1927-382_1927-380del MANE Select	NP_065805.2:n.1927-382_1927-380del