Canonical Allele Identifier: CA1190289486
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709607_114709608delinsCG , CM000663.2:g.114709607_114709608delinsCG GRCh38
NC_000001.10:g.115252228_115252229delinsCG , CM000663.1:g.115252228_115252229delinsCG GRCh37
NC_000001.9:g.115053751_115053752delinsCG NCBI36
NG_007572.1:g.12287_12288delinsCG , LRG_92:g.12287_12288delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.411_412delinsCG MANE Select ENSP00000358548.4:p.Tyr137=
ENST00000369535.4:c.411_412delinsCG ENSP00000358548.4:p.Tyr137=
NM_002524.4:c.411_412delinsCG NP_002515.1:p.Tyr137=
NM_002524.5:c.411_412delinsCG MANE Select NP_002515.1:p.Tyr137=
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