Canonical Allele Identifier: CA362543201
Gene: RACK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.180665146T>C (hg19) chr5:g.181238146T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.181238146T>C , CM000667.2:g.181238146T>C GRCh38
NC_000005.9:g.180665146T>C , CM000667.1:g.180665146T>C GRCh37
NC_000005.8:g.180597752T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000512805.6:c.730A>G MANE Select ENSP00000426909.1:p.Asn244Asp
ENST00000376817.8:c.598A>G ENSP00000366013.4:p.Asn200Asp
ENST00000502844.5:c.688A>G ENSP00000422029.1:p.Asn230Asp
ENST00000502905.5:c.371A>G
ENST00000504128.5:c.449A>G
ENST00000504325.5:c.*383A>G ENSP00000422198.1:n.*383A>G
ENST00000504726.1:c.110-452A>G ENSP00000426046.1:n.110-452A>G
ENST00000507756.5:c.522A>G
ENST00000508682.5:c.*398A>G ENSP00000424760.1:n.*398A>G
ENST00000509148.1:c.50A>G
ENST00000509535.5:c.303A>G
ENST00000510199.5:c.874A>G ENSP00000423569.1:p.Asn292Asp
ENST00000511473.5:c.*622A>G ENSP00000420936.1:n.*622A>G
ENST00000511566.5:c.636+921A>G ENSP00000426101.1:n.636+921A>G
ENST00000511900.5:c.586A>G ENSP00000422768.1:p.Asn196Asp
ENST00000512805.5:c.730A>G ENSP00000426909.1:p.Asn244Asp
ENST00000512968.5:c.784A>G ENSP00000425008.1:p.Asn262Asp
ENST00000513060.5:n.1411A>G
ENST00000514455.5:c.82A>G ENSP00000426708.1:p.Asn28Asp
NM_006098.4:c.730A>G NP_006089.1:p.Asn244Asp
NM_006098.5:c.730A>G MANE Select NP_006089.1:p.Asn244Asp
Search 100 bp 5'
Search 100 bp 3'