Canonical Allele Identifier: CA1190289481
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709587G= , CM000663.2:g.114709587G= GRCh38
NC_000001.10:g.115252208G= , CM000663.1:g.115252208G= GRCh37
NC_000001.9:g.115053731G= NCBI36
NG_007572.1:g.12308C= , LRG_92:g.12308C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.432C= MANE Select ENSP00000358548.4:p.Thr144=
ENST00000369535.4:c.432C= ENSP00000358548.4:p.Thr144=
NM_002524.4:c.432C= NP_002515.1:p.Thr144=
NM_002524.5:c.432C= MANE Select NP_002515.1:p.Thr144=
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