Canonical Allele Identifier: CA354040550

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs61744410
• gnomAD v3: 3-119402370-A-C
• gnomAD v4: 3-119402370-A-C
• MyVariant Identifiers: chr3:g.119121217A>C (hg19) ; chr3:g.119402370A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119402370A>C , CM000665.2:g.119402370A>C	GRCh38
NC_000003.11:g.119121217A>C , CM000665.1:g.119121217A>C	GRCh37
NC_000003.10:g.120603907A>C	NCBI36
NG_007665.2:g.112998A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1618A>C MANE Select	ENSP00000264245.4:p.Lys540Gln
ENST00000264245.8:c.1618A>C	ENSP00000264245.4:p.Lys540Gln
NM_020754.3:c.1618A>C	NP_065805.2:p.Lys540Gln
XM_005247671.3:c.1525A>C	XP_005247728.1:p.Lys509Gln
XM_006713714.2:c.1558A>C	XP_006713777.1:p.Lys520Gln
XM_006713714.3:c.1558A>C	XP_006713777.1:p.Lys520Gln
XM_017006955.1:c.1126A>C	XP_016862444.1:p.Lys376Gln
NM_020754.4:c.1618A>C MANE Select	NP_065805.2:p.Lys540Gln