Canonical Allele Identifier: CA354051177
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414352A>C , CM000665.2:g.119414352A>C GRCh38
NC_000003.11:g.119133199A>C , CM000665.1:g.119133199A>C GRCh37
NC_000003.10:g.120615889A>C NCBI36
NG_007665.2:g.124980A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2423A>C MANE Select ENSP00000264245.4:p.Asp808Ala
ENST00000264245.8:c.2423A>C ENSP00000264245.4:p.Asp808Ala
NM_020754.3:c.2423A>C NP_065805.2:p.Asp808Ala
XM_005247671.3:c.2330A>C XP_005247728.1:p.Asp777Ala
XM_006713714.2:c.2363A>C XP_006713777.1:p.Asp788Ala
XM_006713714.3:c.2363A>C XP_006713777.1:p.Asp788Ala
XM_017006955.1:c.1931A>C XP_016862444.1:p.Asp644Ala
NM_020754.4:c.2423A>C MANE Select NP_065805.2:p.Asp808Ala