Canonical Allele Identifier: CA354050558
Gene: ARHGAP31 HGNC NCBI

Linked Data

COSMIC: COSM73710
MyVariant Identifiers: chr3:g.119133103A>C (hg19) chr3:g.119414256A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414256A>C , CM000665.2:g.119414256A>C GRCh38
NC_000003.11:g.119133103A>C , CM000665.1:g.119133103A>C GRCh37
NC_000003.10:g.120615793A>C NCBI36
NG_007665.2:g.124884A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2327A>C MANE Select ENSP00000264245.4:p.Asn776Thr
ENST00000264245.8:c.2327A>C ENSP00000264245.4:p.Asn776Thr
NM_020754.3:c.2327A>C NP_065805.2:p.Asn776Thr
XM_005247671.3:c.2234A>C XP_005247728.1:p.Asn745Thr
XM_006713714.2:c.2267A>C XP_006713777.1:p.Asn756Thr
XM_006713714.3:c.2267A>C XP_006713777.1:p.Asn756Thr
XM_017006955.1:c.1835A>C XP_016862444.1:p.Asn612Thr
NM_020754.4:c.2327A>C MANE Select NP_065805.2:p.Asn776Thr
Search 100 bp 5'
Search 100 bp 3'