Canonical Allele Identifier: CA354047879
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413883A>C , CM000665.2:g.119413883A>C GRCh38
NC_000003.11:g.119132730A>C , CM000665.1:g.119132730A>C GRCh37
NC_000003.10:g.120615420A>C NCBI36
NG_007665.2:g.124511A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1954A>C MANE Select ENSP00000264245.4:p.Ile652Leu
ENST00000264245.8:c.1954A>C ENSP00000264245.4:p.Ile652Leu
NM_020754.3:c.1954A>C NP_065805.2:p.Ile652Leu
XM_005247671.3:c.1861A>C XP_005247728.1:p.Ile621Leu
XM_006713714.2:c.1894A>C XP_006713777.1:p.Ile632Leu
XM_006713714.3:c.1894A>C XP_006713777.1:p.Ile632Leu
XM_017006955.1:c.1462A>C XP_016862444.1:p.Ile488Leu
NM_020754.4:c.1954A>C MANE Select NP_065805.2:p.Ile652Leu