Canonical Allele Identifier: CA354047930
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413888G>A , CM000665.2:g.119413888G>A GRCh38
NC_000003.11:g.119132735G>A , CM000665.1:g.119132735G>A GRCh37
NC_000003.10:g.120615425G>A NCBI36
NG_007665.2:g.124516G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1959G>A MANE Select ENSP00000264245.4:p.Trp653Ter
ENST00000264245.8:c.1959G>A ENSP00000264245.4:p.Trp653Ter
NM_020754.3:c.1959G>A NP_065805.2:p.Trp653Ter
XM_005247671.3:c.1866G>A XP_005247728.1:p.Trp622Ter
XM_006713714.2:c.1899G>A XP_006713777.1:p.Trp633Ter
XM_006713714.3:c.1899G>A XP_006713777.1:p.Trp633Ter
XM_017006955.1:c.1467G>A XP_016862444.1:p.Trp489Ter
NM_020754.4:c.1959G>A MANE Select NP_065805.2:p.Trp653Ter