Canonical Allele Identifier: CA354057387
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119134040A>C (hg19) chr3:g.119415193A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119415193A>C , CM000665.2:g.119415193A>C GRCh38
NC_000003.11:g.119134040A>C , CM000665.1:g.119134040A>C GRCh37
NC_000003.10:g.120616730A>C NCBI36
NG_007665.2:g.125821A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.3264A>C MANE Select ENSP00000264245.4:p.Leu1088Phe
ENST00000264245.8:c.3264A>C ENSP00000264245.4:p.Leu1088Phe
NM_020754.3:c.3264A>C NP_065805.2:p.Leu1088Phe
XM_005247671.3:c.3171A>C XP_005247728.1:p.Leu1057Phe
XM_006713714.2:c.3204A>C XP_006713777.1:p.Leu1068Phe
XM_006713714.3:c.3204A>C XP_006713777.1:p.Leu1068Phe
XM_017006955.1:c.2772A>C XP_016862444.1:p.Leu924Phe
NM_020754.4:c.3264A>C MANE Select NP_065805.2:p.Leu1088Phe
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