Canonical Allele Identifier: CA1396548453

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413837_119413840delinsGTTT , CM000665.2:g.119413837_119413840delinsGTTT	GRCh38
NC_000003.11:g.119132684_119132687delinsGTTT , CM000665.1:g.119132684_119132687delinsGTTT	GRCh37
NC_000003.10:g.120615374_120615377delinsGTTT	NCBI36
NG_007665.2:g.124465_124468delinsGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-19_1927-16delinsGTTT MANE Select	ENSP00000264245.4:n.1927-19_1927-16delinsGTTT
ENST00000264245.8:c.1927-19_1927-16delinsGTTT	ENSP00000264245.4:n.1927-19_1927-16delinsGTTT
NM_020754.3:c.1927-19_1927-16delinsGTTT	NP_065805.2:n.1927-19_1927-16delinsGTTT
XM_005247671.3:c.1834-19_1834-16delinsGTTT	XP_005247728.1:n.1834-19_1834-16delinsGTTT
XM_006713714.2:c.1867-19_1867-16delinsGTTT	XP_006713777.1:n.1867-19_1867-16delinsGTTT
XM_006713714.3:c.1867-19_1867-16delinsGTTT	XP_006713777.1:n.1867-19_1867-16delinsGTTT
XM_017006955.1:c.1435-19_1435-16delinsGTTT	XP_016862444.1:n.1435-19_1435-16delinsGTTT
NM_020754.4:c.1927-19_1927-16delinsGTTT MANE Select	NP_065805.2:n.1927-19_1927-16delinsGTTT