Canonical Allele Identifier: CA354047874
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1952T>G MANE Select ENSP00000264245.4:p.Leu651Arg
ENST00000264245.8:c.1952T>G ENSP00000264245.4:p.Leu651Arg
NM_020754.3:c.1952T>G NP_065805.2:p.Leu651Arg
XM_005247671.3:c.1859T>G XP_005247728.1:p.Leu620Arg
XM_006713714.2:c.1892T>G XP_006713777.1:p.Leu631Arg
XM_006713714.3:c.1892T>G XP_006713777.1:p.Leu631Arg
XM_017006955.1:c.1460T>G XP_016862444.1:p.Leu487Arg
NM_020754.4:c.1952T>G MANE Select NP_065805.2:p.Leu651Arg