Canonical Allele Identifier: CA354048242

Gene: ARHGAP31

Linked Data

• gnomAD v4: 3-119413934-C-T
• MyVariant Identifiers: chr3:g.119132781C>T (hg19) ; chr3:g.119413934C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413934C>T , CM000665.2:g.119413934C>T	GRCh38
NC_000003.11:g.119132781C>T , CM000665.1:g.119132781C>T	GRCh37
NC_000003.10:g.120615471C>T	NCBI36
NG_007665.2:g.124562C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2005C>T MANE Select	ENSP00000264245.4:p.Leu669Phe
ENST00000264245.8:c.2005C>T	ENSP00000264245.4:p.Leu669Phe
NM_020754.3:c.2005C>T	NP_065805.2:p.Leu669Phe
XM_005247671.3:c.1912C>T	XP_005247728.1:p.Leu638Phe
XM_006713714.2:c.1945C>T	XP_006713777.1:p.Leu649Phe
XM_006713714.3:c.1945C>T	XP_006713777.1:p.Leu649Phe
XM_017006955.1:c.1513C>T	XP_016862444.1:p.Leu505Phe
NM_020754.4:c.2005C>T MANE Select	NP_065805.2:p.Leu669Phe