Canonical Allele Identifier: CA354057356
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119415188A>G , CM000665.2:g.119415188A>G GRCh38
NC_000003.11:g.119134035A>G , CM000665.1:g.119134035A>G GRCh37
NC_000003.10:g.120616725A>G NCBI36
NG_007665.2:g.125816A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.3259A>G MANE Select ENSP00000264245.4:p.Lys1087Glu
ENST00000264245.8:c.3259A>G ENSP00000264245.4:p.Lys1087Glu
NM_020754.3:c.3259A>G NP_065805.2:p.Lys1087Glu
XM_005247671.3:c.3166A>G XP_005247728.1:p.Lys1056Glu
XM_006713714.2:c.3199A>G XP_006713777.1:p.Lys1067Glu
XM_006713714.3:c.3199A>G XP_006713777.1:p.Lys1067Glu
XM_017006955.1:c.2767A>G XP_016862444.1:p.Lys923Glu
NM_020754.4:c.3259A>G MANE Select NP_065805.2:p.Lys1087Glu