Canonical Allele Identifier: CA354047757

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132713A>T (hg19) ; chr3:g.119413866A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413866A>T , CM000665.2:g.119413866A>T	GRCh38
NC_000003.11:g.119132713A>T , CM000665.1:g.119132713A>T	GRCh37
NC_000003.10:g.120615403A>T	NCBI36
NG_007665.2:g.124494A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1937A>T MANE Select	ENSP00000264245.4:p.Asp646Val
ENST00000264245.8:c.1937A>T	ENSP00000264245.4:p.Asp646Val
NM_020754.3:c.1937A>T	NP_065805.2:p.Asp646Val
XM_005247671.3:c.1844A>T	XP_005247728.1:p.Asp615Val
XM_006713714.2:c.1877A>T	XP_006713777.1:p.Asp626Val
XM_006713714.3:c.1877A>T	XP_006713777.1:p.Asp626Val
XM_017006955.1:c.1445A>T	XP_016862444.1:p.Asp482Val
NM_020754.4:c.1937A>T MANE Select	NP_065805.2:p.Asp646Val