Canonical Allele Identifier: CA354051085
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1298931
ClinVar RCV Id: RCV001727261
dbSNP Id: rs2107646911
MyVariant Identifiers: chr3:g.119133186C>A (hg19) chr3:g.119414339C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414339C>A , CM000665.2:g.119414339C>A GRCh38
NC_000003.11:g.119133186C>A , CM000665.1:g.119133186C>A GRCh37
NC_000003.10:g.120615876C>A NCBI36
NG_007665.2:g.124967C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2410C>A MANE Select ENSP00000264245.4:p.Pro804Thr
ENST00000264245.8:c.2410C>A ENSP00000264245.4:p.Pro804Thr
NM_020754.3:c.2410C>A NP_065805.2:p.Pro804Thr
XM_005247671.3:c.2317C>A XP_005247728.1:p.Pro773Thr
XM_006713714.2:c.2350C>A XP_006713777.1:p.Pro784Thr
XM_006713714.3:c.2350C>A XP_006713777.1:p.Pro784Thr
XM_017006955.1:c.1918C>A XP_016862444.1:p.Pro640Thr
NM_020754.4:c.2410C>A MANE Select NP_065805.2:p.Pro804Thr
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