Canonical Allele Identifier: CA2739274823
Gene: RASA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2877034
ClinVar RCV Id: RCV003759505
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268885_87268902delinsA , CM000667.2:g.87268885_87268902delinsA GRCh38
NC_000005.9:g.86564702_86564719delinsA , CM000667.1:g.86564702_86564719delinsA GRCh37
NC_000005.8:g.86600458_86600475delinsA NCBI36
NG_011650.1:g.5552_5569delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.434_451delinsA MANE Select ENSP00000274376.6:p.Pro145GlnfsTer7
ENST00000274376.10:c.434_451delinsA ENSP00000274376.6:p.Pro145GlnfsTer7
ENST00000515800.6:c.434_451delinsA ENSP00000423395.2:p.Pro145GlnfsTer7
NM_002890.2:c.434_451delinsA NP_002881.1:p.Pro145GlnfsTer7
XM_011543525.1:c.434_451delinsA XP_011541827.1:p.Pro145GlnfsTer7
XM_011543526.1:c.434_451delinsA XP_011541828.1:p.Pro145GlnfsTer7
XM_011543527.1:c.434_451delinsA XP_011541829.1:p.Pro145GlnfsTer7
XM_011543525.2:c.434_451delinsA XP_011541827.1:p.Pro145GlnfsTer7
XM_011543527.3:c.434_451delinsA XP_011541829.1:p.Pro145GlnfsTer7
NM_002890.3:c.434_451delinsA MANE Select NP_002881.1:p.Pro145GlnfsTer7
Search 100 bp 5'
Search 100 bp 3'