Canonical Allele Identifier: CA645537996
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713915_114713916insGTTATCCAGTATG , CM000663.2:g.114713915_114713916insGTTATCCAGTATG GRCh38
NC_000001.10:g.115256536_115256537insGTTATCCAGTATG , CM000663.1:g.115256536_115256537insGTTATCCAGTATG GRCh37
NC_000001.9:g.115058059_115058060insGTTATCCAGTATG NCBI36
NG_007572.1:g.7979_7980insCATACTGGATAAC , LRG_92:g.7979_7980insCATACTGGATAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.174_175insCATACTGGATAAC MANE Select ENSP00000358548.4:p.Ala59HisfsTer4
ENST00000369535.4:c.174_175insCATACTGGATAAC ENSP00000358548.4:p.Ala59HisfsTer4
NM_002524.4:c.174_175insCATACTGGATAAC NP_002515.1:p.Ala59HisfsTer4
NM_002524.5:c.174_175insCATACTGGATAAC MANE Select NP_002515.1:p.Ala59HisfsTer4