Canonical Allele Identifier: CA354050671

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119414273-C-T
• MyVariant Identifiers: chr3:g.119133120C>T (hg19) ; chr3:g.119414273C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414273C>T , CM000665.2:g.119414273C>T	GRCh38
NC_000003.11:g.119133120C>T , CM000665.1:g.119133120C>T	GRCh37
NC_000003.10:g.120615810C>T	NCBI36
NG_007665.2:g.124901C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2344C>T MANE Select	ENSP00000264245.4:p.Pro782Ser
ENST00000264245.8:c.2344C>T	ENSP00000264245.4:p.Pro782Ser
NM_020754.3:c.2344C>T	NP_065805.2:p.Pro782Ser
XM_005247671.3:c.2251C>T	XP_005247728.1:p.Pro751Ser
XM_006713714.2:c.2284C>T	XP_006713777.1:p.Pro762Ser
XM_006713714.3:c.2284C>T	XP_006713777.1:p.Pro762Ser
XM_017006955.1:c.1852C>T	XP_016862444.1:p.Pro618Ser
NM_020754.4:c.2344C>T MANE Select	NP_065805.2:p.Pro782Ser