Canonical Allele Identifier: CA2667110268
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119413918-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413919del , CM000665.2:g.119413919del GRCh38
NC_000003.11:g.119132766del , CM000665.1:g.119132766del GRCh37
NC_000003.10:g.120615456del NCBI36
NG_007665.2:g.124547del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1990del MANE Select ENSP00000264245.4:p.Glu664AsnfsTer14
ENST00000264245.8:c.1990del ENSP00000264245.4:p.Glu664AsnfsTer14
NM_020754.3:c.1990del NP_065805.2:p.Glu664AsnfsTer14
XM_005247671.3:c.1897del XP_005247728.1:p.Glu633AsnfsTer14
XM_006713714.2:c.1930del XP_006713777.1:p.Glu644AsnfsTer14
XM_006713714.3:c.1930del XP_006713777.1:p.Glu644AsnfsTer14
XM_017006955.1:c.1498del XP_016862444.1:p.Glu500AsnfsTer14
NM_020754.4:c.1990del MANE Select NP_065805.2:p.Glu664AsnfsTer14
Search 100 bp 5'
Search 100 bp 3'