Canonical Allele Identifier: CA354051626
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133274T>C (hg19) chr3:g.119414427T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414427T>C , CM000665.2:g.119414427T>C GRCh38
NC_000003.11:g.119133274T>C , CM000665.1:g.119133274T>C GRCh37
NC_000003.10:g.120615964T>C NCBI36
NG_007665.2:g.125055T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2498T>C MANE Select ENSP00000264245.4:p.Leu833Pro
ENST00000264245.8:c.2498T>C ENSP00000264245.4:p.Leu833Pro
NM_020754.3:c.2498T>C NP_065805.2:p.Leu833Pro
XM_005247671.3:c.2405T>C XP_005247728.1:p.Leu802Pro
XM_006713714.2:c.2438T>C XP_006713777.1:p.Leu813Pro
XM_006713714.3:c.2438T>C XP_006713777.1:p.Leu813Pro
XM_017006955.1:c.2006T>C XP_016862444.1:p.Leu669Pro
NM_020754.4:c.2498T>C MANE Select NP_065805.2:p.Leu833Pro
Search 100 bp 5'
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