Canonical Allele Identifier: CA354051645
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414431T>G , CM000665.2:g.119414431T>G GRCh38
NC_000003.11:g.119133278T>G , CM000665.1:g.119133278T>G GRCh37
NC_000003.10:g.120615968T>G NCBI36
NG_007665.2:g.125059T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2502T>G MANE Select ENSP00000264245.4:p.Cys834Trp
ENST00000264245.8:c.2502T>G ENSP00000264245.4:p.Cys834Trp
NM_020754.3:c.2502T>G NP_065805.2:p.Cys834Trp
XM_005247671.3:c.2409T>G XP_005247728.1:p.Cys803Trp
XM_006713714.2:c.2442T>G XP_006713777.1:p.Cys814Trp
XM_006713714.3:c.2442T>G XP_006713777.1:p.Cys814Trp
XM_017006955.1:c.2010T>G XP_016862444.1:p.Cys670Trp
NM_020754.4:c.2502T>G MANE Select NP_065805.2:p.Cys834Trp