Canonical Allele Identifier: CA1396548451

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413835_119413836delinsCA , CM000665.2:g.119413835_119413836delinsCA	GRCh38
NC_000003.11:g.119132682_119132683delinsCA , CM000665.1:g.119132682_119132683delinsCA	GRCh37
NC_000003.10:g.120615372_120615373delinsCA	NCBI36
NG_007665.2:g.124463_124464delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-21_1927-20delinsCA MANE Select	ENSP00000264245.4:n.1927-21_1927-20delinsCA
ENST00000264245.8:c.1927-21_1927-20delinsCA	ENSP00000264245.4:n.1927-21_1927-20delinsCA
NM_020754.3:c.1927-21_1927-20delinsCA	NP_065805.2:n.1927-21_1927-20delinsCA
XM_005247671.3:c.1834-21_1834-20delinsCA	XP_005247728.1:n.1834-21_1834-20delinsCA
XM_006713714.2:c.1867-21_1867-20delinsCA	XP_006713777.1:n.1867-21_1867-20delinsCA
XM_006713714.3:c.1867-21_1867-20delinsCA	XP_006713777.1:n.1867-21_1867-20delinsCA
XM_017006955.1:c.1435-21_1435-20delinsCA	XP_016862444.1:n.1435-21_1435-20delinsCA
NM_020754.4:c.1927-21_1927-20delinsCA MANE Select	NP_065805.2:n.1927-21_1927-20delinsCA