Canonical Allele Identifier: CA897778740

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1270436898
• MyVariant Identifiers: chr3:g.119132491_119132493del (hg19) ; chr3:g.119413644_119413646del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413644_119413646del , CM000665.2:g.119413644_119413646del	GRCh38
NC_000003.11:g.119132491_119132493del , CM000665.1:g.119132491_119132493del	GRCh37
NC_000003.10:g.120615181_120615183del	NCBI36
NG_007665.2:g.124272_124274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-212_1927-210del MANE Select	ENSP00000264245.4:n.1927-212_1927-210del
ENST00000264245.8:c.1927-212_1927-210del	ENSP00000264245.4:n.1927-212_1927-210del
NM_020754.3:c.1927-212_1927-210del	NP_065805.2:n.1927-212_1927-210del
XM_005247671.3:c.1834-212_1834-210del	XP_005247728.1:n.1834-212_1834-210del
XM_006713714.2:c.1867-212_1867-210del	XP_006713777.1:n.1867-212_1867-210del
XM_006713714.3:c.1867-212_1867-210del	XP_006713777.1:n.1867-212_1867-210del
XM_017006955.1:c.1435-212_1435-210del	XP_016862444.1:n.1435-212_1435-210del
NM_020754.4:c.1927-212_1927-210del MANE Select	NP_065805.2:n.1927-212_1927-210del