Canonical Allele Identifier: CA2647252960

Gene: NRAS

Linked Data

• gnomAD v4: 1-114709433-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709433_114709434insC , CM000663.2:g.114709433_114709434insC	GRCh38
NC_000001.10:g.115252054_115252055insC , CM000663.1:g.115252054_115252055insC	GRCh37
NC_000001.9:g.115053577_115053578insC	NCBI36
NG_007572.1:g.12461_12462insG , LRG_92:g.12461_12462insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+135_450+136insG MANE Select	ENSP00000358548.4:n.450+135_450+136insG
ENST00000369535.4:c.450+135_450+136insG	ENSP00000358548.4:n.450+135_450+136insG
NM_002524.4:c.450+135_450+136insG	NP_002515.1:n.450+135_450+136insG
NM_002524.5:c.450+135_450+136insG MANE Select	NP_002515.1:n.450+135_450+136insG