Canonical Allele Identifier: CA1190289419
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658991310
gnomAD v4: 1-114709443-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709449dup , CM000663.2:g.114709449dup GRCh38
NC_000001.10:g.115252070dup , CM000663.1:g.115252070dup GRCh37
NC_000001.9:g.115053593dup NCBI36
NG_007572.1:g.12451dup , LRG_92:g.12451dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+125dup MANE Select ENSP00000358548.4:n.450+125dup
ENST00000369535.4:c.450+125dup ENSP00000358548.4:n.450+125dup
NM_002524.4:c.450+125dup NP_002515.1:n.450+125dup
NM_002524.5:c.450+125dup MANE Select NP_002515.1:n.450+125dup
Search 100 bp 5'
Search 100 bp 3'