Canonical Allele Identifier: CA354048104
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413911A>C , CM000665.2:g.119413911A>C GRCh38
NC_000003.11:g.119132758A>C , CM000665.1:g.119132758A>C GRCh37
NC_000003.10:g.120615448A>C NCBI36
NG_007665.2:g.124539A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1982A>C MANE Select ENSP00000264245.4:p.Lys661Thr
ENST00000264245.8:c.1982A>C ENSP00000264245.4:p.Lys661Thr
NM_020754.3:c.1982A>C NP_065805.2:p.Lys661Thr
XM_005247671.3:c.1889A>C XP_005247728.1:p.Lys630Thr
XM_006713714.2:c.1922A>C XP_006713777.1:p.Lys641Thr
XM_006713714.3:c.1922A>C XP_006713777.1:p.Lys641Thr
XM_017006955.1:c.1490A>C XP_016862444.1:p.Lys497Thr
NM_020754.4:c.1982A>C MANE Select NP_065805.2:p.Lys661Thr