Canonical Allele Identifier: CA1052740022

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs2080741028
• gnomAD v3: 3-119413837-GTTT-G
• gnomAD v4: 3-119413837-GTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413838_119413840del , CM000665.2:g.119413838_119413840del	GRCh38
NC_000003.11:g.119132685_119132687del , CM000665.1:g.119132685_119132687del	GRCh37
NC_000003.10:g.120615375_120615377del	NCBI36
NG_007665.2:g.124466_124468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-18_1927-16del MANE Select	ENSP00000264245.4:n.1927-18_1927-16del
ENST00000264245.8:c.1927-18_1927-16del	ENSP00000264245.4:n.1927-18_1927-16del
NM_020754.3:c.1927-18_1927-16del	NP_065805.2:n.1927-18_1927-16del
XM_005247671.3:c.1834-18_1834-16del	XP_005247728.1:n.1834-18_1834-16del
XM_006713714.2:c.1867-18_1867-16del	XP_006713777.1:n.1867-18_1867-16del
XM_006713714.3:c.1867-18_1867-16del	XP_006713777.1:n.1867-18_1867-16del
XM_017006955.1:c.1435-18_1435-16del	XP_016862444.1:n.1435-18_1435-16del
NM_020754.4:c.1927-18_1927-16del MANE Select	NP_065805.2:n.1927-18_1927-16del