Canonical Allele Identifier: CA1396548466
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413877_119413878delinsGC , CM000665.2:g.119413877_119413878delinsGC GRCh38
NC_000003.11:g.119132724_119132725delinsGC , CM000665.1:g.119132724_119132725delinsGC GRCh37
NC_000003.10:g.120615414_120615415delinsGC NCBI36
NG_007665.2:g.124505_124506delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1948_1949delinsGC MANE Select ENSP00000264245.4:p.Ala650=
ENST00000264245.8:c.1948_1949delinsGC ENSP00000264245.4:p.Ala650=
NM_020754.3:c.1948_1949delinsGC NP_065805.2:p.Ala650=
XM_005247671.3:c.1855_1856delinsGC XP_005247728.1:p.Ala619=
XM_006713714.2:c.1888_1889delinsGC XP_006713777.1:p.Ala630=
XM_006713714.3:c.1888_1889delinsGC XP_006713777.1:p.Ala630=
XM_017006955.1:c.1456_1457delinsGC XP_016862444.1:p.Ala486=
NM_020754.4:c.1948_1949delinsGC MANE Select NP_065805.2:p.Ala650=