Canonical Allele Identifier: CA354047893
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413884T>G , CM000665.2:g.119413884T>G GRCh38
NC_000003.11:g.119132731T>G , CM000665.1:g.119132731T>G GRCh37
NC_000003.10:g.120615421T>G NCBI36
NG_007665.2:g.124512T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1955T>G MANE Select ENSP00000264245.4:p.Ile652Ser
ENST00000264245.8:c.1955T>G ENSP00000264245.4:p.Ile652Ser
NM_020754.3:c.1955T>G NP_065805.2:p.Ile652Ser
XM_005247671.3:c.1862T>G XP_005247728.1:p.Ile621Ser
XM_006713714.2:c.1895T>G XP_006713777.1:p.Ile632Ser
XM_006713714.3:c.1895T>G XP_006713777.1:p.Ile632Ser
XM_017006955.1:c.1463T>G XP_016862444.1:p.Ile488Ser
NM_020754.4:c.1955T>G MANE Select NP_065805.2:p.Ile652Ser