Canonical Allele Identifier: CA1396548311

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413468_119413471delinsTTTG , CM000665.2:g.119413468_119413471delinsTTTG	GRCh38
NC_000003.11:g.119132315_119132318delinsTTTG , CM000665.1:g.119132315_119132318delinsTTTG	GRCh37
NC_000003.10:g.120615005_120615008delinsTTTG	NCBI36
NG_007665.2:g.124096_124099delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-388_1927-385delinsTTTG MANE Select	ENSP00000264245.4:n.1927-388_1927-385delinsTTTG
ENST00000264245.8:c.1927-388_1927-385delinsTTTG	ENSP00000264245.4:n.1927-388_1927-385delinsTTTG
NM_020754.3:c.1927-388_1927-385delinsTTTG	NP_065805.2:n.1927-388_1927-385delinsTTTG
XM_005247671.3:c.1834-388_1834-385delinsTTTG	XP_005247728.1:n.1834-388_1834-385delinsTTTG
XM_006713714.2:c.1867-388_1867-385delinsTTTG	XP_006713777.1:n.1867-388_1867-385delinsTTTG
XM_006713714.3:c.1867-388_1867-385delinsTTTG	XP_006713777.1:n.1867-388_1867-385delinsTTTG
XM_017006955.1:c.1435-388_1435-385delinsTTTG	XP_016862444.1:n.1435-388_1435-385delinsTTTG
NM_020754.4:c.1927-388_1927-385delinsTTTG MANE Select	NP_065805.2:n.1927-388_1927-385delinsTTTG