Canonical Allele Identifier: CA2647253744
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709741_114709745del , CM000663.2:g.114709741_114709745del GRCh38
NC_000001.10:g.115252362_115252366del , CM000663.1:g.115252362_115252366del GRCh37
NC_000001.9:g.115053885_115053889del NCBI36
NG_007572.1:g.12151_12155del , LRG_92:g.12151_12155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-16_291-12del MANE Select ENSP00000358548.4:n.291-16_291-12del
ENST00000369535.4:c.291-16_291-12del ENSP00000358548.4:n.291-16_291-12del
NM_002524.4:c.291-16_291-12del NP_002515.1:n.291-16_291-12del
NM_002524.5:c.291-16_291-12del MANE Select NP_002515.1:n.291-16_291-12del