Canonical Allele Identifier: CA897778885

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1445628182
• MyVariant Identifiers: chr3:g.119132683_119132686del (hg19) ; chr3:g.119413836_119413839del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413836_119413839del , CM000665.2:g.119413836_119413839del	GRCh38
NC_000003.11:g.119132683_119132686del , CM000665.1:g.119132683_119132686del	GRCh37
NC_000003.10:g.120615373_120615376del	NCBI36
NG_007665.2:g.124464_124467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-20_1927-17del MANE Select	ENSP00000264245.4:n.1927-20_1927-17del
ENST00000264245.8:c.1927-20_1927-17del	ENSP00000264245.4:n.1927-20_1927-17del
NM_020754.3:c.1927-20_1927-17del	NP_065805.2:n.1927-20_1927-17del
XM_005247671.3:c.1834-20_1834-17del	XP_005247728.1:n.1834-20_1834-17del
XM_006713714.2:c.1867-20_1867-17del	XP_006713777.1:n.1867-20_1867-17del
XM_006713714.3:c.1867-20_1867-17del	XP_006713777.1:n.1867-20_1867-17del
XM_017006955.1:c.1435-20_1435-17del	XP_016862444.1:n.1435-20_1435-17del
NM_020754.4:c.1927-20_1927-17del MANE Select	NP_065805.2:n.1927-20_1927-17del