Canonical Allele Identifier: CA435209488
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119121225G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402378G>T , CM000665.2:g.119402378G>T GRCh38
NC_000003.11:g.119121225G>T , CM000665.1:g.119121225G>T GRCh37
NC_000003.10:g.120603915G>T NCBI36
NG_007665.2:g.113006G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1626G>T MANE Select ENSP00000264245.4:p.Leu542=
ENST00000264245.8:c.1626G>T ENSP00000264245.4:p.Leu542=
NM_020754.3:c.1626G>T NP_065805.2:p.Leu542=
XM_005247671.3:c.1533G>T XP_005247728.1:p.Leu511=
XM_006713714.2:c.1566G>T XP_006713777.1:p.Leu522=
XM_006713714.3:c.1566G>T XP_006713777.1:p.Leu522=
XM_017006955.1:c.1134G>T XP_016862444.1:p.Leu378=
NM_020754.4:c.1626G>T MANE Select NP_065805.2:p.Leu542=