Canonical Allele Identifier: CA354050346
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414219T>C , CM000665.2:g.119414219T>C GRCh38
NC_000003.11:g.119133066T>C , CM000665.1:g.119133066T>C GRCh37
NC_000003.10:g.120615756T>C NCBI36
NG_007665.2:g.124847T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2290T>C MANE Select ENSP00000264245.4:p.Ser764Pro
ENST00000264245.8:c.2290T>C ENSP00000264245.4:p.Ser764Pro
NM_020754.3:c.2290T>C NP_065805.2:p.Ser764Pro
XM_005247671.3:c.2197T>C XP_005247728.1:p.Ser733Pro
XM_006713714.2:c.2230T>C XP_006713777.1:p.Ser744Pro
XM_006713714.3:c.2230T>C XP_006713777.1:p.Ser744Pro
XM_017006955.1:c.1798T>C XP_016862444.1:p.Ser600Pro
NM_020754.4:c.2290T>C MANE Select NP_065805.2:p.Ser764Pro