Canonical Allele Identifier: CA1396548448
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413835_119413839delinsCAGTT , CM000665.2:g.119413835_119413839delinsCAGTT GRCh38
NC_000003.11:g.119132682_119132686delinsCAGTT , CM000665.1:g.119132682_119132686delinsCAGTT GRCh37
NC_000003.10:g.120615372_120615376delinsCAGTT NCBI36
NG_007665.2:g.124463_124467delinsCAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1927-21_1927-17delinsCAGTT MANE Select ENSP00000264245.4:n.1927-21_1927-17delinsCAGTT
ENST00000264245.8:c.1927-21_1927-17delinsCAGTT ENSP00000264245.4:n.1927-21_1927-17delinsCAGTT
NM_020754.3:c.1927-21_1927-17delinsCAGTT NP_065805.2:n.1927-21_1927-17delinsCAGTT
XM_005247671.3:c.1834-21_1834-17delinsCAGTT XP_005247728.1:n.1834-21_1834-17delinsCAGTT
XM_006713714.2:c.1867-21_1867-17delinsCAGTT XP_006713777.1:n.1867-21_1867-17delinsCAGTT
XM_006713714.3:c.1867-21_1867-17delinsCAGTT XP_006713777.1:n.1867-21_1867-17delinsCAGTT
XM_017006955.1:c.1435-21_1435-17delinsCAGTT XP_016862444.1:n.1435-21_1435-17delinsCAGTT
NM_020754.4:c.1927-21_1927-17delinsCAGTT MANE Select NP_065805.2:n.1927-21_1927-17delinsCAGTT