Canonical Allele Identifier: CA354051226
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414363A>G , CM000665.2:g.119414363A>G GRCh38
NC_000003.11:g.119133210A>G , CM000665.1:g.119133210A>G GRCh37
NC_000003.10:g.120615900A>G NCBI36
NG_007665.2:g.124991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2434A>G MANE Select ENSP00000264245.4:p.Lys812Glu
ENST00000264245.8:c.2434A>G ENSP00000264245.4:p.Lys812Glu
NM_020754.3:c.2434A>G NP_065805.2:p.Lys812Glu
XM_005247671.3:c.2341A>G XP_005247728.1:p.Lys781Glu
XM_006713714.2:c.2374A>G XP_006713777.1:p.Lys792Glu
XM_006713714.3:c.2374A>G XP_006713777.1:p.Lys792Glu
XM_017006955.1:c.1942A>G XP_016862444.1:p.Lys648Glu
NM_020754.4:c.2434A>G MANE Select NP_065805.2:p.Lys812Glu