Canonical Allele Identifier: CA408424229
Gene: CST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23618346C>G (hg19) chr20:g.23637709C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637709C>G , CM000682.2:g.23637709C>G GRCh38
NC_000020.10:g.23618346C>G , CM000682.1:g.23618346C>G GRCh37
NC_000020.9:g.23566346C>G NCBI36
NG_012887.2:g.5229G>C
NG_012887.3:g.5229G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.154G>C MANE Select ENSP00000366124.3:p.Ala52Pro
ENST00000376925.7:c.154G>C ENSP00000366124.3:p.Ala52Pro
ENST00000398409.1:c.154G>C ENSP00000381446.1:p.Ala52Pro
ENST00000398411.5:c.154G>C ENSP00000381448.1:p.Ala52Pro
NM_000099.3:c.154G>C NP_000090.1:p.Ala52Pro
NM_001288614.1:c.154G>C NP_001275543.1:p.Ala52Pro
NM_000099.4:c.154G>C MANE Select NP_000090.1:p.Ala52Pro
NM_001288614.2:c.154G>C NP_001275543.1:p.Ala52Pro
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