Canonical Allele Identifier: CA1396548622

Gene: ARHGAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414261_119414264delinsTCTC , CM000665.2:g.119414261_119414264delinsTCTC	GRCh38
NC_000003.11:g.119133108_119133111delinsTCTC , CM000665.1:g.119133108_119133111delinsTCTC	GRCh37
NC_000003.10:g.120615798_120615801delinsTCTC	NCBI36
NG_007665.2:g.124889_124892delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2332_2335delinsTCTC MANE Select	ENSP00000264245.4:p.Ser778=
ENST00000264245.8:c.2332_2335delinsTCTC	ENSP00000264245.4:p.Ser778=
NM_020754.3:c.2332_2335delinsTCTC	NP_065805.2:p.Ser778=
XM_005247671.3:c.2239_2242delinsTCTC	XP_005247728.1:p.Ser747=
XM_006713714.2:c.2272_2275delinsTCTC	XP_006713777.1:p.Ser758=
XM_006713714.3:c.2272_2275delinsTCTC	XP_006713777.1:p.Ser758=
XM_017006955.1:c.1840_1843delinsTCTC	XP_016862444.1:p.Ser614=
NM_020754.4:c.2332_2335delinsTCTC MANE Select	NP_065805.2:p.Ser778=