Canonical Allele Identifier: CA354047942
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413889C>A , CM000665.2:g.119413889C>A GRCh38
NC_000003.11:g.119132736C>A , CM000665.1:g.119132736C>A GRCh37
NC_000003.10:g.120615426C>A NCBI36
NG_007665.2:g.124517C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1960C>A MANE Select ENSP00000264245.4:p.Pro654Thr
ENST00000264245.8:c.1960C>A ENSP00000264245.4:p.Pro654Thr
NM_020754.3:c.1960C>A NP_065805.2:p.Pro654Thr
XM_005247671.3:c.1867C>A XP_005247728.1:p.Pro623Thr
XM_006713714.2:c.1900C>A XP_006713777.1:p.Pro634Thr
XM_006713714.3:c.1900C>A XP_006713777.1:p.Pro634Thr
XM_017006955.1:c.1468C>A XP_016862444.1:p.Pro490Thr
NM_020754.4:c.1960C>A MANE Select NP_065805.2:p.Pro654Thr