Canonical Allele Identifier: CA1396543743

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs2080617988

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119402270_119402271insGTGGGCGGCGTGCCGGTGCGGCTGGAAA , CM000665.2:g.119402270_119402271insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	GRCh38
NC_000003.11:g.119121117_119121118insGTGGGCGGCGTGCCGGTGCGGCTGGAAA , CM000665.1:g.119121117_119121118insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	GRCh37
NC_000003.10:g.120603807_120603808insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	NCBI36
NG_007665.2:g.112898_112899insGTGGGCGGCGTGCCGGTGCGGCTGGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1518_1519insGTGGGCGGCGTGCCGGTGCGGCTGGAAA MANE Select	ENSP00000264245.4:p.Thr507ValfsTer?
ENST00000264245.8:c.1518_1519insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	ENSP00000264245.4:p.Thr507ValfsTer?
NM_020754.3:c.1518_1519insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	NP_065805.2:p.Thr507ValfsTer?
XM_005247671.3:c.1425_1426insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	XP_005247728.1:p.Thr476ValfsTer?
XM_006713714.2:c.1458_1459insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	XP_006713777.1:p.Thr487ValfsTer?
XM_006713714.3:c.1458_1459insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	XP_006713777.1:p.Thr487ValfsTer?
XM_017006955.1:c.1026_1027insGTGGGCGGCGTGCCGGTGCGGCTGGAAA	XP_016862444.1:p.Thr343ValfsTer?
NM_020754.4:c.1518_1519insGTGGGCGGCGTGCCGGTGCGGCTGGAAA MANE Select	NP_065805.2:p.Thr507ValfsTer?