Canonical Allele Identifier: CA354047896
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413886T>C , CM000665.2:g.119413886T>C GRCh38
NC_000003.11:g.119132733T>C , CM000665.1:g.119132733T>C GRCh37
NC_000003.10:g.120615423T>C NCBI36
NG_007665.2:g.124514T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1957T>C MANE Select ENSP00000264245.4:p.Trp653Arg
ENST00000264245.8:c.1957T>C ENSP00000264245.4:p.Trp653Arg
NM_020754.3:c.1957T>C NP_065805.2:p.Trp653Arg
XM_005247671.3:c.1864T>C XP_005247728.1:p.Trp622Arg
XM_006713714.2:c.1897T>C XP_006713777.1:p.Trp633Arg
XM_006713714.3:c.1897T>C XP_006713777.1:p.Trp633Arg
XM_017006955.1:c.1465T>C XP_016862444.1:p.Trp489Arg
NM_020754.4:c.1957T>C MANE Select NP_065805.2:p.Trp653Arg