Canonical Allele Identifier: CA435209476
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119121219A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402372A>G , CM000665.2:g.119402372A>G GRCh38
NC_000003.11:g.119121219A>G , CM000665.1:g.119121219A>G GRCh37
NC_000003.10:g.120603909A>G NCBI36
NG_007665.2:g.113000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1620A>G MANE Select ENSP00000264245.4:p.Lys540=
ENST00000264245.8:c.1620A>G ENSP00000264245.4:p.Lys540=
NM_020754.3:c.1620A>G NP_065805.2:p.Lys540=
XM_005247671.3:c.1527A>G XP_005247728.1:p.Lys509=
XM_006713714.2:c.1560A>G XP_006713777.1:p.Lys520=
XM_006713714.3:c.1560A>G XP_006713777.1:p.Lys520=
XM_017006955.1:c.1128A>G XP_016862444.1:p.Lys376=
NM_020754.4:c.1620A>G MANE Select NP_065805.2:p.Lys540=