Canonical Allele Identifier: CA2554038
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs763998234

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414355C>T , CM000665.2:g.119414355C>T GRCh38
NC_000003.11:g.119133202C>T , CM000665.1:g.119133202C>T GRCh37
NC_000003.10:g.120615892C>T NCBI36
NG_007665.2:g.124983C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2426C>T MANE Select ENSP00000264245.4:p.Ser809Leu
ENST00000264245.8:c.2426C>T ENSP00000264245.4:p.Ser809Leu
NM_020754.3:c.2426C>T NP_065805.2:p.Ser809Leu
XM_005247671.3:c.2333C>T XP_005247728.1:p.Ser778Leu
XM_006713714.2:c.2366C>T XP_006713777.1:p.Ser789Leu
XM_006713714.3:c.2366C>T XP_006713777.1:p.Ser789Leu
XM_017006955.1:c.1934C>T XP_016862444.1:p.Ser645Leu
NM_020754.4:c.2426C>T MANE Select NP_065805.2:p.Ser809Leu