Canonical Allele Identifier: CA354051137
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414347A>C , CM000665.2:g.119414347A>C GRCh38
NC_000003.11:g.119133194A>C , CM000665.1:g.119133194A>C GRCh37
NC_000003.10:g.120615884A>C NCBI36
NG_007665.2:g.124975A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2418A>C MANE Select ENSP00000264245.4:p.Arg806Ser
ENST00000264245.8:c.2418A>C ENSP00000264245.4:p.Arg806Ser
NM_020754.3:c.2418A>C NP_065805.2:p.Arg806Ser
XM_005247671.3:c.2325A>C XP_005247728.1:p.Arg775Ser
XM_006713714.2:c.2358A>C XP_006713777.1:p.Arg786Ser
XM_006713714.3:c.2358A>C XP_006713777.1:p.Arg786Ser
XM_017006955.1:c.1926A>C XP_016862444.1:p.Arg642Ser
NM_020754.4:c.2418A>C MANE Select NP_065805.2:p.Arg806Ser