Canonical Allele Identifier: CA354047833
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413876T>A , CM000665.2:g.119413876T>A GRCh38
NC_000003.11:g.119132723T>A , CM000665.1:g.119132723T>A GRCh37
NC_000003.10:g.120615413T>A NCBI36
NG_007665.2:g.124504T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1947T>A MANE Select ENSP00000264245.4:p.Asn649Lys
ENST00000264245.8:c.1947T>A ENSP00000264245.4:p.Asn649Lys
NM_020754.3:c.1947T>A NP_065805.2:p.Asn649Lys
XM_005247671.3:c.1854T>A XP_005247728.1:p.Asn618Lys
XM_006713714.2:c.1887T>A XP_006713777.1:p.Asn629Lys
XM_006713714.3:c.1887T>A XP_006713777.1:p.Asn629Lys
XM_017006955.1:c.1455T>A XP_016862444.1:p.Asn485Lys
NM_020754.4:c.1947T>A MANE Select NP_065805.2:p.Asn649Lys