Canonical Allele Identifier: CA2577942209
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414375_119414384del , CM000665.2:g.119414375_119414384del GRCh38
NC_000003.11:g.119133222_119133231del , CM000665.1:g.119133222_119133231del GRCh37
NC_000003.10:g.120615912_120615921del NCBI36
NG_007665.2:g.125003_125012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2446_2455del MANE Select ENSP00000264245.4:p.Asp816Ter
ENST00000264245.8:c.2446_2455del ENSP00000264245.4:p.Asp816Ter
NM_020754.3:c.2446_2455del NP_065805.2:p.Asp816Ter
XM_005247671.3:c.2353_2362del XP_005247728.1:p.Asp785Ter
XM_006713714.2:c.2386_2395del XP_006713777.1:p.Asp796Ter
XM_006713714.3:c.2386_2395del XP_006713777.1:p.Asp796Ter
XM_017006955.1:c.1954_1963del XP_016862444.1:p.Asp652Ter
NM_020754.4:c.2446_2455del MANE Select NP_065805.2:p.Asp816Ter