Canonical Allele Identifier: CA354050498
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414246G>A , CM000665.2:g.119414246G>A GRCh38
NC_000003.11:g.119133093G>A , CM000665.1:g.119133093G>A GRCh37
NC_000003.10:g.120615783G>A NCBI36
NG_007665.2:g.124874G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2317G>A MANE Select ENSP00000264245.4:p.Gly773Ser
ENST00000264245.8:c.2317G>A ENSP00000264245.4:p.Gly773Ser
NM_020754.3:c.2317G>A NP_065805.2:p.Gly773Ser
XM_005247671.3:c.2224G>A XP_005247728.1:p.Gly742Ser
XM_006713714.2:c.2257G>A XP_006713777.1:p.Gly753Ser
XM_006713714.3:c.2257G>A XP_006713777.1:p.Gly753Ser
XM_017006955.1:c.1825G>A XP_016862444.1:p.Gly609Ser
NM_020754.4:c.2317G>A MANE Select NP_065805.2:p.Gly773Ser