Canonical Allele Identifier: CA354047878

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132730A>T (hg19) ; chr3:g.119413883A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413883A>T , CM000665.2:g.119413883A>T	GRCh38
NC_000003.11:g.119132730A>T , CM000665.1:g.119132730A>T	GRCh37
NC_000003.10:g.120615420A>T	NCBI36
NG_007665.2:g.124511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1954A>T MANE Select	ENSP00000264245.4:p.Ile652Phe
ENST00000264245.8:c.1954A>T	ENSP00000264245.4:p.Ile652Phe
NM_020754.3:c.1954A>T	NP_065805.2:p.Ile652Phe
XM_005247671.3:c.1861A>T	XP_005247728.1:p.Ile621Phe
XM_006713714.2:c.1894A>T	XP_006713777.1:p.Ile632Phe
XM_006713714.3:c.1894A>T	XP_006713777.1:p.Ile632Phe
XM_017006955.1:c.1462A>T	XP_016862444.1:p.Ile488Phe
NM_020754.4:c.1954A>T MANE Select	NP_065805.2:p.Ile652Phe