Canonical Allele Identifier: CA354047869
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1951C>G MANE Select ENSP00000264245.4:p.Leu651Val
ENST00000264245.8:c.1951C>G ENSP00000264245.4:p.Leu651Val
NM_020754.3:c.1951C>G NP_065805.2:p.Leu651Val
XM_005247671.3:c.1858C>G XP_005247728.1:p.Leu620Val
XM_006713714.2:c.1891C>G XP_006713777.1:p.Leu631Val
XM_006713714.3:c.1891C>G XP_006713777.1:p.Leu631Val
XM_017006955.1:c.1459C>G XP_016862444.1:p.Leu487Val
NM_020754.4:c.1951C>G MANE Select NP_065805.2:p.Leu651Val