Canonical Allele Identifier: CA354048041
Gene: ARHGAP31 HGNC NCBI

Linked Data

COSMIC: COSM359828

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413901C>A , CM000665.2:g.119413901C>A GRCh38
NC_000003.11:g.119132748C>A , CM000665.1:g.119132748C>A GRCh37
NC_000003.10:g.120615438C>A NCBI36
NG_007665.2:g.124529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1972C>A MANE Select ENSP00000264245.4:p.Gln658Lys
ENST00000264245.8:c.1972C>A ENSP00000264245.4:p.Gln658Lys
NM_020754.3:c.1972C>A NP_065805.2:p.Gln658Lys
XM_005247671.3:c.1879C>A XP_005247728.1:p.Gln627Lys
XM_006713714.2:c.1912C>A XP_006713777.1:p.Gln638Lys
XM_006713714.3:c.1912C>A XP_006713777.1:p.Gln638Lys
XM_017006955.1:c.1480C>A XP_016862444.1:p.Gln494Lys
NM_020754.4:c.1972C>A MANE Select NP_065805.2:p.Gln658Lys