Canonical Allele Identifier: CA633644818
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1353208084
gnomAD v2: 19-50139850-T-TC
gnomAD v4: 19-49636593-T-TC
MyVariant Identifiers: chr19:g.50139850_50139851insC (hg19) chr19:g.49636593_49636594insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636597dup , CM000681.2:g.49636597dup GRCh38
NC_000019.9:g.50139854dup , CM000681.1:g.50139854dup GRCh37
NC_000019.8:g.54831666dup NCBI36
NG_042222.1:g.8550dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+25dup MANE Select ENSP00000246792.2:n.453+25dup
ENST00000246792.3:c.453+25dup ENSP00000246792.2:n.453+25dup
ENST00000601532.1:n.593+25dup
NM_006270.3:c.453+25dup NP_006261.1:n.453+25dup
NM_006270.4:c.453+25dup NP_006261.1:n.453+25dup
NM_006270.5:c.453+25dup MANE Select NP_006261.1:n.453+25dup
Search 100 bp 5'
Search 100 bp 3'