Canonical Allele Identifier: CA354049642
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414109C>G , CM000665.2:g.119414109C>G GRCh38
NC_000003.11:g.119132956C>G , CM000665.1:g.119132956C>G GRCh37
NC_000003.10:g.120615646C>G NCBI36
NG_007665.2:g.124737C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2180C>G MANE Select ENSP00000264245.4:p.Thr727Arg
ENST00000264245.8:c.2180C>G ENSP00000264245.4:p.Thr727Arg
NM_020754.3:c.2180C>G NP_065805.2:p.Thr727Arg
XM_005247671.3:c.2087C>G XP_005247728.1:p.Thr696Arg
XM_006713714.2:c.2120C>G XP_006713777.1:p.Thr707Arg
XM_006713714.3:c.2120C>G XP_006713777.1:p.Thr707Arg
XM_017006955.1:c.1688C>G XP_016862444.1:p.Thr563Arg
NM_020754.4:c.2180C>G MANE Select NP_065805.2:p.Thr727Arg