Canonical Allele Identifier: CA354048149
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413920A>G , CM000665.2:g.119413920A>G GRCh38
NC_000003.11:g.119132767A>G , CM000665.1:g.119132767A>G GRCh37
NC_000003.10:g.120615457A>G NCBI36
NG_007665.2:g.124548A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1991A>G MANE Select ENSP00000264245.4:p.Glu664Gly
ENST00000264245.8:c.1991A>G ENSP00000264245.4:p.Glu664Gly
NM_020754.3:c.1991A>G NP_065805.2:p.Glu664Gly
XM_005247671.3:c.1898A>G XP_005247728.1:p.Glu633Gly
XM_006713714.2:c.1931A>G XP_006713777.1:p.Glu644Gly
XM_006713714.3:c.1931A>G XP_006713777.1:p.Glu644Gly
XM_017006955.1:c.1499A>G XP_016862444.1:p.Glu500Gly
NM_020754.4:c.1991A>G MANE Select NP_065805.2:p.Glu664Gly