Canonical Allele Identifier: CA1396548420
Gene: ARHGAP31 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413775C= , CM000665.2:g.119413775C= GRCh38
NC_000003.11:g.119132622C= , CM000665.1:g.119132622C= GRCh37
NC_000003.10:g.120615312C= NCBI36
NG_007665.2:g.124403C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1927-81C= MANE Select ENSP00000264245.4:n.1927-81C=
ENST00000264245.8:c.1927-81C= ENSP00000264245.4:n.1927-81C=
NM_020754.3:c.1927-81C= NP_065805.2:n.1927-81C=
XM_005247671.3:c.1834-81C= XP_005247728.1:n.1834-81C=
XM_006713714.2:c.1867-81C= XP_006713777.1:n.1867-81C=
XM_006713714.3:c.1867-81C= XP_006713777.1:n.1867-81C=
XM_017006955.1:c.1435-81C= XP_016862444.1:n.1435-81C=
NM_020754.4:c.1927-81C= MANE Select NP_065805.2:n.1927-81C=
Search 100 bp 5'
Search 100 bp 3'