Canonical Allele Identifier: CA1005998384
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658990204
gnomAD v3: 1-114709416-T-TA
gnomAD v4: 1-114709416-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709417dup , CM000663.2:g.114709417dup GRCh38
NC_000001.10:g.115252038dup , CM000663.1:g.115252038dup GRCh37
NC_000001.9:g.115053561dup NCBI36
NG_007572.1:g.12478dup , LRG_92:g.12478dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+152dup MANE Select ENSP00000358548.4:n.450+152dup
ENST00000369535.4:c.450+152dup ENSP00000358548.4:n.450+152dup
NM_002524.4:c.450+152dup NP_002515.1:n.450+152dup
NM_002524.5:c.450+152dup MANE Select NP_002515.1:n.450+152dup
Search 100 bp 5'
Search 100 bp 3'