Canonical Allele Identifier: CA354047862
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413880C>A , CM000665.2:g.119413880C>A GRCh38
NC_000003.11:g.119132727C>A , CM000665.1:g.119132727C>A GRCh37
NC_000003.10:g.120615417C>A NCBI36
NG_007665.2:g.124508C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1951C>A MANE Select ENSP00000264245.4:p.Leu651Met
ENST00000264245.8:c.1951C>A ENSP00000264245.4:p.Leu651Met
NM_020754.3:c.1951C>A NP_065805.2:p.Leu651Met
XM_005247671.3:c.1858C>A XP_005247728.1:p.Leu620Met
XM_006713714.2:c.1891C>A XP_006713777.1:p.Leu631Met
XM_006713714.3:c.1891C>A XP_006713777.1:p.Leu631Met
XM_017006955.1:c.1459C>A XP_016862444.1:p.Leu487Met
NM_020754.4:c.1951C>A MANE Select NP_065805.2:p.Leu651Met