Canonical Allele Identifier: CA2758108463
Gene: ARHGAP31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414380_119414381insAA , CM000665.2:g.119414380_119414381insAA GRCh38
NC_000003.11:g.119133227_119133228insAA , CM000665.1:g.119133227_119133228insAA GRCh37
NC_000003.10:g.120615917_120615918insAA NCBI36
NG_007665.2:g.125008_125009insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2451_2452insAA MANE Select ENSP00000264245.4:p.Tyr818AsnfsTer3
ENST00000264245.8:c.2451_2452insAA ENSP00000264245.4:p.Tyr818AsnfsTer3
NM_020754.3:c.2451_2452insAA NP_065805.2:p.Tyr818AsnfsTer3
XM_005247671.3:c.2358_2359insAA XP_005247728.1:p.Tyr787AsnfsTer3
XM_006713714.2:c.2391_2392insAA XP_006713777.1:p.Tyr798AsnfsTer3
XM_006713714.3:c.2391_2392insAA XP_006713777.1:p.Tyr798AsnfsTer3
XM_017006955.1:c.1959_1960insAA XP_016862444.1:p.Tyr654AsnfsTer3
NM_020754.4:c.2451_2452insAA MANE Select NP_065805.2:p.Tyr818AsnfsTer3
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