Canonical Allele Identifier: CA408424158
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637677T>G , CM000682.2:g.23637677T>G GRCh38
NC_000020.10:g.23618314T>G , CM000682.1:g.23618314T>G GRCh37
NC_000020.9:g.23566314T>G NCBI36
NG_012887.2:g.5261A>C
NG_012887.3:g.5261A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.186A>C MANE Select ENSP00000366124.3:p.Lys62Asn
ENST00000376925.7:c.186A>C ENSP00000366124.3:p.Lys62Asn
ENST00000398409.1:c.186A>C ENSP00000381446.1:p.Lys62Asn
ENST00000398411.5:c.186A>C ENSP00000381448.1:p.Lys62Asn
NM_000099.3:c.186A>C NP_000090.1:p.Lys62Asn
NM_001288614.1:c.186A>C NP_001275543.1:p.Lys62Asn
NM_000099.4:c.186A>C MANE Select NP_000090.1:p.Lys62Asn
NM_001288614.2:c.186A>C NP_001275543.1:p.Lys62Asn