Canonical Allele Identifier: CA354051463
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414398G>C , CM000665.2:g.119414398G>C GRCh38
NC_000003.11:g.119133245G>C , CM000665.1:g.119133245G>C GRCh37
NC_000003.10:g.120615935G>C NCBI36
NG_007665.2:g.125026G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2469G>C MANE Select ENSP00000264245.4:p.Lys823Asn
ENST00000264245.8:c.2469G>C ENSP00000264245.4:p.Lys823Asn
NM_020754.3:c.2469G>C NP_065805.2:p.Lys823Asn
XM_005247671.3:c.2376G>C XP_005247728.1:p.Lys792Asn
XM_006713714.2:c.2409G>C XP_006713777.1:p.Lys803Asn
XM_006713714.3:c.2409G>C XP_006713777.1:p.Lys803Asn
XM_017006955.1:c.1977G>C XP_016862444.1:p.Lys659Asn
NM_020754.4:c.2469G>C MANE Select NP_065805.2:p.Lys823Asn