Canonical Allele Identifier: CA81697356
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs201379699

Genomic Alleles

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

Transcript Alleles

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