Canonical Allele Identifier: CA1396548498
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413979C= , CM000665.2:g.119413979C= GRCh38
NC_000003.11:g.119132826C= , CM000665.1:g.119132826C= GRCh37
NC_000003.10:g.120615516C= NCBI36
NG_007665.2:g.124607C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.2050C= MANE Select ENSP00000264245.4:p.Pro684=
ENST00000264245.8:c.2050C= ENSP00000264245.4:p.Pro684=
NM_020754.3:c.2050C= NP_065805.2:p.Pro684=
XM_005247671.3:c.1957C= XP_005247728.1:p.Pro653=
XM_006713714.2:c.1990C= XP_006713777.1:p.Pro664=
XM_006713714.3:c.1990C= XP_006713777.1:p.Pro664=
XM_017006955.1:c.1558C= XP_016862444.1:p.Pro520=
NM_020754.4:c.2050C= MANE Select NP_065805.2:p.Pro684=