Canonical Allele Identifier: CA354050399
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414228G>C , CM000665.2:g.119414228G>C GRCh38
NC_000003.11:g.119133075G>C , CM000665.1:g.119133075G>C GRCh37
NC_000003.10:g.120615765G>C NCBI36
NG_007665.2:g.124856G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2299G>C MANE Select ENSP00000264245.4:p.Ala767Pro
ENST00000264245.8:c.2299G>C ENSP00000264245.4:p.Ala767Pro
NM_020754.3:c.2299G>C NP_065805.2:p.Ala767Pro
XM_005247671.3:c.2206G>C XP_005247728.1:p.Ala736Pro
XM_006713714.2:c.2239G>C XP_006713777.1:p.Ala747Pro
XM_006713714.3:c.2239G>C XP_006713777.1:p.Ala747Pro
XM_017006955.1:c.1807G>C XP_016862444.1:p.Ala603Pro
NM_020754.4:c.2299G>C MANE Select NP_065805.2:p.Ala767Pro