Canonical Allele Identifier: CA1396548467
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs2080741338

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413880del , CM000665.2:g.119413880del GRCh38
NC_000003.11:g.119132727del , CM000665.1:g.119132727del GRCh37
NC_000003.10:g.120615417del NCBI36
NG_007665.2:g.124508del

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1951del MANE Select ENSP00000264245.4:p.Leu651Ter
ENST00000264245.8:c.1951del ENSP00000264245.4:p.Leu651Ter
NM_020754.3:c.1951del NP_065805.2:p.Leu651Ter
XM_005247671.3:c.1858del XP_005247728.1:p.Leu620Ter
XM_006713714.2:c.1891del XP_006713777.1:p.Leu631Ter
XM_006713714.3:c.1891del XP_006713777.1:p.Leu631Ter
XM_017006955.1:c.1459del XP_016862444.1:p.Leu487Ter
NM_020754.4:c.1951del MANE Select NP_065805.2:p.Leu651Ter