Canonical Allele Identifier: CA354051494
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133253A>C (hg19) chr3:g.119414406A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414406A>C , CM000665.2:g.119414406A>C GRCh38
NC_000003.11:g.119133253A>C , CM000665.1:g.119133253A>C GRCh37
NC_000003.10:g.120615943A>C NCBI36
NG_007665.2:g.125034A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2477A>C MANE Select ENSP00000264245.4:p.Asp826Ala
ENST00000264245.8:c.2477A>C ENSP00000264245.4:p.Asp826Ala
NM_020754.3:c.2477A>C NP_065805.2:p.Asp826Ala
XM_005247671.3:c.2384A>C XP_005247728.1:p.Asp795Ala
XM_006713714.2:c.2417A>C XP_006713777.1:p.Asp806Ala
XM_006713714.3:c.2417A>C XP_006713777.1:p.Asp806Ala
XM_017006955.1:c.1985A>C XP_016862444.1:p.Asp662Ala
NM_020754.4:c.2477A>C MANE Select NP_065805.2:p.Asp826Ala
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