Canonical Allele Identifier: CA435412155

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133248C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414401C>T , CM000665.2:g.119414401C>T	GRCh38
NC_000003.11:g.119133248C>T , CM000665.1:g.119133248C>T	GRCh37
NC_000003.10:g.120615938C>T	NCBI36
NG_007665.2:g.125029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2472C>T MANE Select	ENSP00000264245.4:p.Ser824=
ENST00000264245.8:c.2472C>T	ENSP00000264245.4:p.Ser824=
NM_020754.3:c.2472C>T	NP_065805.2:p.Ser824=
XM_005247671.3:c.2379C>T	XP_005247728.1:p.Ser793=
XM_006713714.2:c.2412C>T	XP_006713777.1:p.Ser804=
XM_006713714.3:c.2412C>T	XP_006713777.1:p.Ser804=
XM_017006955.1:c.1980C>T	XP_016862444.1:p.Ser660=
NM_020754.4:c.2472C>T MANE Select	NP_065805.2:p.Ser824=