Canonical Allele Identifier: CA510163485
Gene: CST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23618338G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637701G>A , CM000682.2:g.23637701G>A GRCh38
NC_000020.10:g.23618338G>A , CM000682.1:g.23618338G>A GRCh37
NC_000020.9:g.23566338G>A NCBI36
NG_012887.2:g.5237C>T
NG_012887.3:g.5237C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.162C>T MANE Select ENSP00000366124.3:p.Asp54=
ENST00000376925.7:c.162C>T ENSP00000366124.3:p.Asp54=
ENST00000398409.1:c.162C>T ENSP00000381446.1:p.Asp54=
ENST00000398411.5:c.162C>T ENSP00000381448.1:p.Asp54=
NM_000099.3:c.162C>T NP_000090.1:p.Asp54=
NM_001288614.1:c.162C>T NP_001275543.1:p.Asp54=
NM_000099.4:c.162C>T MANE Select NP_000090.1:p.Asp54=
NM_001288614.2:c.162C>T NP_001275543.1:p.Asp54=