Canonical Allele Identifier: CA354049219
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414042G>T , CM000665.2:g.119414042G>T GRCh38
NC_000003.11:g.119132889G>T , CM000665.1:g.119132889G>T GRCh37
NC_000003.10:g.120615579G>T NCBI36
NG_007665.2:g.124670G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2113G>T MANE Select ENSP00000264245.4:p.Gly705Cys
ENST00000264245.8:c.2113G>T ENSP00000264245.4:p.Gly705Cys
NM_020754.3:c.2113G>T NP_065805.2:p.Gly705Cys
XM_005247671.3:c.2020G>T XP_005247728.1:p.Gly674Cys
XM_006713714.2:c.2053G>T XP_006713777.1:p.Gly685Cys
XM_006713714.3:c.2053G>T XP_006713777.1:p.Gly685Cys
XM_017006955.1:c.1621G>T XP_016862444.1:p.Gly541Cys
NM_020754.4:c.2113G>T MANE Select NP_065805.2:p.Gly705Cys