Canonical Allele Identifier: CA885826346
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1187593941
gnomAD v3: 1-114705901-T-TAAA
gnomAD v4: 1-114705901-T-TAAA
MyVariant Identifiers: chr1:g.115248522_115248523insAAA (hg19) chr1:g.114705901_114705902insAAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705902_114705903insAAA , CM000663.2:g.114705902_114705903insAAA GRCh38
NC_000001.10:g.115248523_115248524insAAA , CM000663.1:g.115248523_115248524insAAA GRCh37
NC_000001.9:g.115050046_115050047insAAA NCBI36
NG_007572.1:g.15993_15994insTTT , LRG_92:g.15993_15994insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2192_*2193insTTT MANE Select ENSP00000358548.4:n.*2192_*2193insTTT
ENST00000369535.4:c.*2192_*2193insTTT ENSP00000358548.4:n.*2192_*2193insTTT
NM_002524.4:c.*2192_*2193insTTT NP_002515.1:n.*2192_*2193insTTT
NM_002524.5:c.*2192_*2193insTTT MANE Select NP_002515.1:n.*2192_*2193insTTT
Search 100 bp 5'
Search 100 bp 3'