Canonical Allele Identifier: CA885828045

Gene: NRAS

Linked Data

• dbSNP Id: rs1334489247
• gnomAD v3: 1-114709456-AATAAAAAT-A
• gnomAD v4: 1-114709456-AATAAAAAT-A
• MyVariant Identifiers: chr1:g.115252078_115252085del (hg19) ; chr1:g.114709457_114709464del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709457_114709464del , CM000663.2:g.114709457_114709464del	GRCh38
NC_000001.10:g.115252078_115252085del , CM000663.1:g.115252078_115252085del	GRCh37
NC_000001.9:g.115053601_115053608del	NCBI36
NG_007572.1:g.12431_12438del , LRG_92:g.12431_12438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+105_450+112del MANE Select	ENSP00000358548.4:n.450+105_450+112del
ENST00000369535.4:c.450+105_450+112del	ENSP00000358548.4:n.450+105_450+112del
NM_002524.4:c.450+105_450+112del	NP_002515.1:n.450+105_450+112del
NM_002524.5:c.450+105_450+112del MANE Select	NP_002515.1:n.450+105_450+112del