Canonical Allele Identifier: CA354048624
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413978G>C , CM000665.2:g.119413978G>C GRCh38
NC_000003.11:g.119132825G>C , CM000665.1:g.119132825G>C GRCh37
NC_000003.10:g.120615515G>C NCBI36
NG_007665.2:g.124606G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.2049G>C MANE Select ENSP00000264245.4:p.Gln683His
ENST00000264245.8:c.2049G>C ENSP00000264245.4:p.Gln683His
NM_020754.3:c.2049G>C NP_065805.2:p.Gln683His
XM_005247671.3:c.1956G>C XP_005247728.1:p.Gln652His
XM_006713714.2:c.1989G>C XP_006713777.1:p.Gln663His
XM_006713714.3:c.1989G>C XP_006713777.1:p.Gln663His
XM_017006955.1:c.1557G>C XP_016862444.1:p.Gln519His
NM_020754.4:c.2049G>C MANE Select NP_065805.2:p.Gln683His