Canonical Allele Identifier: CA510163488
Gene: CST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23618343G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637706G>A , CM000682.2:g.23637706G>A GRCh38
NC_000020.10:g.23618343G>A , CM000682.1:g.23618343G>A GRCh37
NC_000020.9:g.23566343G>A NCBI36
NG_012887.2:g.5232C>T
NG_012887.3:g.5232C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.157C>T MANE Select ENSP00000366124.3:p.Leu53=
ENST00000376925.7:c.157C>T ENSP00000366124.3:p.Leu53=
ENST00000398409.1:c.157C>T ENSP00000381446.1:p.Leu53=
ENST00000398411.5:c.157C>T ENSP00000381448.1:p.Leu53=
NM_000099.3:c.157C>T NP_000090.1:p.Leu53=
NM_001288614.1:c.157C>T NP_001275543.1:p.Leu53=
NM_000099.4:c.157C>T MANE Select NP_000090.1:p.Leu53=
NM_001288614.2:c.157C>T NP_001275543.1:p.Leu53=
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