Canonical Allele Identifier: CA1396543787
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402370A= , CM000665.2:g.119402370A= GRCh38
NC_000003.11:g.119121217A= , CM000665.1:g.119121217A= GRCh37
NC_000003.10:g.120603907A= NCBI36
NG_007665.2:g.112998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1618A= MANE Select ENSP00000264245.4:p.Lys540=
ENST00000264245.8:c.1618A= ENSP00000264245.4:p.Lys540=
NM_020754.3:c.1618A= NP_065805.2:p.Lys540=
XM_005247671.3:c.1525A= XP_005247728.1:p.Lys509=
XM_006713714.2:c.1558A= XP_006713777.1:p.Lys520=
XM_006713714.3:c.1558A= XP_006713777.1:p.Lys520=
XM_017006955.1:c.1126A= XP_016862444.1:p.Lys376=
NM_020754.4:c.1618A= MANE Select NP_065805.2:p.Lys540=