Canonical Allele Identifier: CA2667109881
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119402369-GAAA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402370_119402372del , CM000665.2:g.119402370_119402372del GRCh38
NC_000003.11:g.119121217_119121219del , CM000665.1:g.119121217_119121219del GRCh37
NC_000003.10:g.120603907_120603909del NCBI36
NG_007665.2:g.112998_113000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1618_1620del MANE Select ENSP00000264245.4:p.Lys540del
ENST00000264245.8:c.1618_1620del ENSP00000264245.4:p.Lys540del
NM_020754.3:c.1618_1620del NP_065805.2:p.Lys540del
XM_005247671.3:c.1525_1527del XP_005247728.1:p.Lys509del
XM_006713714.2:c.1558_1560del XP_006713777.1:p.Lys520del
XM_006713714.3:c.1558_1560del XP_006713777.1:p.Lys520del
XM_017006955.1:c.1126_1128del XP_016862444.1:p.Lys376del
NM_020754.4:c.1618_1620del MANE Select NP_065805.2:p.Lys540del
Search 100 bp 5'
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