Canonical Allele Identifier: CA354050969

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133160C>G (hg19) ; chr3:g.119414313C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414313C>G , CM000665.2:g.119414313C>G	GRCh38
NC_000003.11:g.119133160C>G , CM000665.1:g.119133160C>G	GRCh37
NC_000003.10:g.120615850C>G	NCBI36
NG_007665.2:g.124941C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2384C>G MANE Select	ENSP00000264245.4:p.Thr795Ser
ENST00000264245.8:c.2384C>G	ENSP00000264245.4:p.Thr795Ser
NM_020754.3:c.2384C>G	NP_065805.2:p.Thr795Ser
XM_005247671.3:c.2291C>G	XP_005247728.1:p.Thr764Ser
XM_006713714.2:c.2324C>G	XP_006713777.1:p.Thr775Ser
XM_006713714.3:c.2324C>G	XP_006713777.1:p.Thr775Ser
XM_017006955.1:c.1892C>G	XP_016862444.1:p.Thr631Ser
NM_020754.4:c.2384C>G MANE Select	NP_065805.2:p.Thr795Ser