Canonical Allele Identifier: CA354047965
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413890C>A , CM000665.2:g.119413890C>A GRCh38
NC_000003.11:g.119132737C>A , CM000665.1:g.119132737C>A GRCh37
NC_000003.10:g.120615427C>A NCBI36
NG_007665.2:g.124518C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1961C>A MANE Select ENSP00000264245.4:p.Pro654His
ENST00000264245.8:c.1961C>A ENSP00000264245.4:p.Pro654His
NM_020754.3:c.1961C>A NP_065805.2:p.Pro654His
XM_005247671.3:c.1868C>A XP_005247728.1:p.Pro623His
XM_006713714.2:c.1901C>A XP_006713777.1:p.Pro634His
XM_006713714.3:c.1901C>A XP_006713777.1:p.Pro634His
XM_017006955.1:c.1469C>A XP_016862444.1:p.Pro490His
NM_020754.4:c.1961C>A MANE Select NP_065805.2:p.Pro654His