Canonical Allele Identifier: CA354050862

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119133144C>T (hg19) ; chr3:g.119414297C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414297C>T , CM000665.2:g.119414297C>T	GRCh38
NC_000003.11:g.119133144C>T , CM000665.1:g.119133144C>T	GRCh37
NC_000003.10:g.120615834C>T	NCBI36
NG_007665.2:g.124925C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2368C>T MANE Select	ENSP00000264245.4:p.Pro790Ser
ENST00000264245.8:c.2368C>T	ENSP00000264245.4:p.Pro790Ser
NM_020754.3:c.2368C>T	NP_065805.2:p.Pro790Ser
XM_005247671.3:c.2275C>T	XP_005247728.1:p.Pro759Ser
XM_006713714.2:c.2308C>T	XP_006713777.1:p.Pro770Ser
XM_006713714.3:c.2308C>T	XP_006713777.1:p.Pro770Ser
XM_017006955.1:c.1876C>T	XP_016862444.1:p.Pro626Ser
NM_020754.4:c.2368C>T MANE Select	NP_065805.2:p.Pro790Ser