Canonical Allele Identifier: CA354050708
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133126G>C (hg19) chr3:g.119414279G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414279G>C , CM000665.2:g.119414279G>C GRCh38
NC_000003.11:g.119133126G>C , CM000665.1:g.119133126G>C GRCh37
NC_000003.10:g.120615816G>C NCBI36
NG_007665.2:g.124907G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2350G>C MANE Select ENSP00000264245.4:p.Ala784Pro
ENST00000264245.8:c.2350G>C ENSP00000264245.4:p.Ala784Pro
NM_020754.3:c.2350G>C NP_065805.2:p.Ala784Pro
XM_005247671.3:c.2257G>C XP_005247728.1:p.Ala753Pro
XM_006713714.2:c.2290G>C XP_006713777.1:p.Ala764Pro
XM_006713714.3:c.2290G>C XP_006713777.1:p.Ala764Pro
XM_017006955.1:c.1858G>C XP_016862444.1:p.Ala620Pro
NM_020754.4:c.2350G>C MANE Select NP_065805.2:p.Ala784Pro
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