Canonical Allele Identifier: CA2553958
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs201379699

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413987C>G , CM000665.2:g.119413987C>G GRCh38
NC_000003.11:g.119132834C>G , CM000665.1:g.119132834C>G GRCh37
NC_000003.10:g.120615524C>G NCBI36
NG_007665.2:g.124615C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.2058C>G MANE Select ENSP00000264245.4:p.Leu686=
ENST00000264245.8:c.2058C>G ENSP00000264245.4:p.Leu686=
NM_020754.3:c.2058C>G NP_065805.2:p.Leu686=
XM_005247671.3:c.1965C>G XP_005247728.1:p.Leu655=
XM_006713714.2:c.1998C>G XP_006713777.1:p.Leu666=
XM_006713714.3:c.1998C>G XP_006713777.1:p.Leu666=
XM_017006955.1:c.1566C>G XP_016862444.1:p.Leu522=
NM_020754.4:c.2058C>G MANE Select NP_065805.2:p.Leu686=