Canonical Allele Identifier: CA545960928

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1403599674
• gnomAD v2: 3-119132647-AT-A
• gnomAD v3: 3-119413800-AT-A
• gnomAD v4: 3-119413800-AT-A
• MyVariant Identifiers: chr3:g.119132648del (hg19) ; chr3:g.119413801del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413801del , CM000665.2:g.119413801del	GRCh38
NC_000003.11:g.119132648del , CM000665.1:g.119132648del	GRCh37
NC_000003.10:g.120615338del	NCBI36
NG_007665.2:g.124429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-55del MANE Select	ENSP00000264245.4:n.1927-55del
ENST00000264245.8:c.1927-55del	ENSP00000264245.4:n.1927-55del
NM_020754.3:c.1927-55del	NP_065805.2:n.1927-55del
XM_005247671.3:c.1834-55del	XP_005247728.1:n.1834-55del
XM_006713714.2:c.1867-55del	XP_006713777.1:n.1867-55del
XM_006713714.3:c.1867-55del	XP_006713777.1:n.1867-55del
XM_017006955.1:c.1435-55del	XP_016862444.1:n.1435-55del
NM_020754.4:c.1927-55del MANE Select	NP_065805.2:n.1927-55del