Canonical Allele Identifier: CA1005998437

Gene: NRAS

Linked Data

• dbSNP Id: rs1658994659
• gnomAD v3: 1-114709527-C-CTGATGCAAACTCTTGCACAAATGCTGAAAGCTGTACCATACCTGTCTGGTCTTGGCTGAGGTTTCAATG
• gnomAD v4: 1-114709527-C-CTGATGCAAACTCTTGCACAAATGCTGAAAGCTGTACCATACCTGTCTGGTCTTGGCTGAGGTTTCAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709528_114709596dup , CM000663.2:g.114709528_114709596dup	GRCh38
NC_000001.10:g.115252149_115252217dup , CM000663.1:g.115252149_115252217dup	GRCh37
NC_000001.9:g.115053672_115053740dup	NCBI36
NG_007572.1:g.12299_12367dup , LRG_92:g.12299_12367dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.423_450+41dup
ENST00000369535.4:c.423_450+41dup
NM_002524.4:c.423_450+41dup
NM_002524.5:c.423_450+41dup