Canonical Allele Identifier: CA81697309

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs905945409
• MyVariant Identifiers: chr3:g.119132812del (hg19) ; chr3:g.119413965del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413966del , CM000665.2:g.119413966del	GRCh38
NC_000003.11:g.119132813del , CM000665.1:g.119132813del	GRCh37
NC_000003.10:g.120615503del	NCBI36
NG_007665.2:g.124594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2037del MANE Select	ENSP00000264245.4:p.Ser680AlafsTer?
ENST00000264245.8:c.2037del	ENSP00000264245.4:p.Ser680AlafsTer?
NM_020754.3:c.2037del	NP_065805.2:p.Ser680AlafsTer?
XM_005247671.3:c.1944del	XP_005247728.1:p.Ser649AlafsTer?
XM_006713714.2:c.1977del	XP_006713777.1:p.Ser660AlafsTer?
XM_006713714.3:c.1977del	XP_006713777.1:p.Ser660AlafsTer?
XM_017006955.1:c.1545del	XP_016862444.1:p.Ser516AlafsTer?
NM_020754.4:c.2037del MANE Select	NP_065805.2:p.Ser680AlafsTer?