Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA341741350

Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256442A>G (hg19) chr1:g.114713821A>G (hg38)

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Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713821A>G , CM000663.2:g.114713821A>G	GRCh38
NC_000001.10:g.115256442A>G , CM000663.1:g.115256442A>G	GRCh37
NC_000001.9:g.115057965A>G	NCBI36
NG_007572.1:g.8074T>C , LRG_92:g.8074T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.269T>C MANE Select	ENSP00000358548.4:p.Phe90Ser
ENST00000369535.4:c.269T>C	ENSP00000358548.4:p.Phe90Ser
NM_002524.4:c.269T>C	NP_002515.1:p.Phe90Ser
NM_002524.5:c.269T>C MANE Select	NP_002515.1:p.Phe90Ser

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