Canonical Allele Identifier: CA1396543790
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402375G= , CM000665.2:g.119402375G= GRCh38
NC_000003.11:g.119121222G= , CM000665.1:g.119121222G= GRCh37
NC_000003.10:g.120603912G= NCBI36
NG_007665.2:g.113003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1623G= MANE Select ENSP00000264245.4:p.Pro541=
ENST00000264245.8:c.1623G= ENSP00000264245.4:p.Pro541=
NM_020754.3:c.1623G= NP_065805.2:p.Pro541=
XM_005247671.3:c.1530G= XP_005247728.1:p.Pro510=
XM_006713714.2:c.1563G= XP_006713777.1:p.Pro521=
XM_006713714.3:c.1563G= XP_006713777.1:p.Pro521=
XM_017006955.1:c.1131G= XP_016862444.1:p.Pro377=
NM_020754.4:c.1623G= MANE Select NP_065805.2:p.Pro541=