Canonical Allele Identifier: CA435412172

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133941A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119415094A>C , CM000665.2:g.119415094A>C	GRCh38
NC_000003.11:g.119133941A>C , CM000665.1:g.119133941A>C	GRCh37
NC_000003.10:g.120616631A>C	NCBI36
NG_007665.2:g.125722A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.3165A>C MANE Select	ENSP00000264245.4:p.Pro1055=
ENST00000264245.8:c.3165A>C	ENSP00000264245.4:p.Pro1055=
NM_020754.3:c.3165A>C	NP_065805.2:p.Pro1055=
XM_005247671.3:c.3072A>C	XP_005247728.1:p.Pro1024=
XM_006713714.2:c.3105A>C	XP_006713777.1:p.Pro1035=
XM_006713714.3:c.3105A>C	XP_006713777.1:p.Pro1035=
XM_017006955.1:c.2673A>C	XP_016862444.1:p.Pro891=
NM_020754.4:c.3165A>C MANE Select	NP_065805.2:p.Pro1055=