Canonical Allele Identifier: CA354047857
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413878C>A , CM000665.2:g.119413878C>A GRCh38
NC_000003.11:g.119132725C>A , CM000665.1:g.119132725C>A GRCh37
NC_000003.10:g.120615415C>A NCBI36
NG_007665.2:g.124506C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1949C>A MANE Select ENSP00000264245.4:p.Ala650Asp
ENST00000264245.8:c.1949C>A ENSP00000264245.4:p.Ala650Asp
NM_020754.3:c.1949C>A NP_065805.2:p.Ala650Asp
XM_005247671.3:c.1856C>A XP_005247728.1:p.Ala619Asp
XM_006713714.2:c.1889C>A XP_006713777.1:p.Ala630Asp
XM_006713714.3:c.1889C>A XP_006713777.1:p.Ala630Asp
XM_017006955.1:c.1457C>A XP_016862444.1:p.Ala486Asp
NM_020754.4:c.1949C>A MANE Select NP_065805.2:p.Ala650Asp