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: CA341741307

Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256433A>C (hg19) chr1:g.114713812A>C (hg38)

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Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713812A>C , CM000663.2:g.114713812A>C	GRCh38
NC_000001.10:g.115256433A>C , CM000663.1:g.115256433A>C	GRCh37
NC_000001.9:g.115057956A>C	NCBI36
NG_007572.1:g.8083T>G , LRG_92:g.8083T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.278T>G MANE Select	ENSP00000358548.4:p.Ile93Ser
ENST00000369535.4:c.278T>G	ENSP00000358548.4:p.Ile93Ser
NM_002524.4:c.278T>G	NP_002515.1:p.Ile93Ser
NM_002524.5:c.278T>G MANE Select	NP_002515.1:p.Ile93Ser

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