Canonical Allele Identifier: CA354040588

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119121220C>G (hg19) ; chr3:g.119402373C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119402373C>G , CM000665.2:g.119402373C>G	GRCh38
NC_000003.11:g.119121220C>G , CM000665.1:g.119121220C>G	GRCh37
NC_000003.10:g.120603910C>G	NCBI36
NG_007665.2:g.113001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1621C>G MANE Select	ENSP00000264245.4:p.Pro541Ala
ENST00000264245.8:c.1621C>G	ENSP00000264245.4:p.Pro541Ala
NM_020754.3:c.1621C>G	NP_065805.2:p.Pro541Ala
XM_005247671.3:c.1528C>G	XP_005247728.1:p.Pro510Ala
XM_006713714.2:c.1561C>G	XP_006713777.1:p.Pro521Ala
XM_006713714.3:c.1561C>G	XP_006713777.1:p.Pro521Ala
XM_017006955.1:c.1129C>G	XP_016862444.1:p.Pro377Ala
NM_020754.4:c.1621C>G MANE Select	NP_065805.2:p.Pro541Ala