Canonical Allele Identifier: CA354051028
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133177A>C (hg19) chr3:g.119414330A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414330A>C , CM000665.2:g.119414330A>C GRCh38
NC_000003.11:g.119133177A>C , CM000665.1:g.119133177A>C GRCh37
NC_000003.10:g.120615867A>C NCBI36
NG_007665.2:g.124958A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2401A>C MANE Select ENSP00000264245.4:p.Lys801Gln
ENST00000264245.8:c.2401A>C ENSP00000264245.4:p.Lys801Gln
NM_020754.3:c.2401A>C NP_065805.2:p.Lys801Gln
XM_005247671.3:c.2308A>C XP_005247728.1:p.Lys770Gln
XM_006713714.2:c.2341A>C XP_006713777.1:p.Lys781Gln
XM_006713714.3:c.2341A>C XP_006713777.1:p.Lys781Gln
XM_017006955.1:c.1909A>C XP_016862444.1:p.Lys637Gln
NM_020754.4:c.2401A>C MANE Select NP_065805.2:p.Lys801Gln
Search 100 bp 5'
Search 100 bp 3'