Canonical Allele Identifier: CA658657456
Gene: RASA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268846_87268847delinsTT , CM000667.2:g.87268846_87268847delinsTT GRCh38
NC_000005.9:g.86564663_86564664delinsTT , CM000667.1:g.86564663_86564664delinsTT GRCh37
NC_000005.8:g.86600419_86600420delinsTT NCBI36
NG_011650.1:g.5513_5514delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.395_396delinsTT MANE Select ENSP00000274376.6:p.Gly132Val
ENST00000274376.10:c.395_396delinsTT ENSP00000274376.6:p.Gly132Val
ENST00000515800.6:c.395_396delinsTT ENSP00000423395.2:p.Gly132Val
NM_002890.2:c.395_396delinsTT NP_002881.1:p.Gly132Val
XM_011543525.1:c.395_396delinsTT XP_011541827.1:p.Gly132Val
XM_011543526.1:c.395_396delinsTT XP_011541828.1:p.Gly132Val
XM_011543527.1:c.395_396delinsTT XP_011541829.1:p.Gly132Val
XM_011543525.2:c.395_396delinsTT XP_011541827.1:p.Gly132Val
XM_011543527.3:c.395_396delinsTT XP_011541829.1:p.Gly132Val
NM_002890.3:c.395_396delinsTT MANE Select NP_002881.1:p.Gly132Val