Canonical Allele Identifier: CA354057350

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119134033C>T (hg19) ; chr3:g.119415186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415186C>T , CM000665.2:g.119415186C>T	GRCh38
NC_000003.11:g.119134033C>T , CM000665.1:g.119134033C>T	GRCh37
NC_000003.10:g.120616723C>T	NCBI36
NG_007665.2:g.125814C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3257C>T MANE Select	ENSP00000264245.4:p.Ala1086Val
ENST00000264245.8:c.3257C>T	ENSP00000264245.4:p.Ala1086Val
NM_020754.3:c.3257C>T	NP_065805.2:p.Ala1086Val
XM_005247671.3:c.3164C>T	XP_005247728.1:p.Ala1055Val
XM_006713714.2:c.3197C>T	XP_006713777.1:p.Ala1066Val
XM_006713714.3:c.3197C>T	XP_006713777.1:p.Ala1066Val
XM_017006955.1:c.2765C>T	XP_016862444.1:p.Ala922Val
NM_020754.4:c.3257C>T MANE Select	NP_065805.2:p.Ala1086Val