Canonical Allele Identifier: CA1396548469
Gene: ARHGAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413881T= , CM000665.2:g.119413881T= GRCh38
NC_000003.11:g.119132728T= , CM000665.1:g.119132728T= GRCh37
NC_000003.10:g.120615418T= NCBI36
NG_007665.2:g.124509T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1952T= MANE Select ENSP00000264245.4:p.Leu651=
ENST00000264245.8:c.1952T= ENSP00000264245.4:p.Leu651=
NM_020754.3:c.1952T= NP_065805.2:p.Leu651=
XM_005247671.3:c.1859T= XP_005247728.1:p.Leu620=
XM_006713714.2:c.1892T= XP_006713777.1:p.Leu631=
XM_006713714.3:c.1892T= XP_006713777.1:p.Leu631=
XM_017006955.1:c.1460T= XP_016862444.1:p.Leu487=
NM_020754.4:c.1952T= MANE Select NP_065805.2:p.Leu651=