Canonical Allele Identifier: CA2667110273
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119414390-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414391del , CM000665.2:g.119414391del GRCh38
NC_000003.11:g.119133238del , CM000665.1:g.119133238del GRCh37
NC_000003.10:g.120615928del NCBI36
NG_007665.2:g.125019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2462del MANE Select ENSP00000264245.4:p.Gln821ArgfsTer2
ENST00000264245.8:c.2462del ENSP00000264245.4:p.Gln821ArgfsTer2
NM_020754.3:c.2462del NP_065805.2:p.Gln821ArgfsTer2
XM_005247671.3:c.2369del XP_005247728.1:p.Gln790ArgfsTer2
XM_006713714.2:c.2402del XP_006713777.1:p.Gln801ArgfsTer2
XM_006713714.3:c.2402del XP_006713777.1:p.Gln801ArgfsTer2
XM_017006955.1:c.1970del XP_016862444.1:p.Gln657ArgfsTer2
NM_020754.4:c.2462del MANE Select NP_065805.2:p.Gln821ArgfsTer2
Search 100 bp 5'
Search 100 bp 3'