Canonical Allele Identifier: CA408424135

Gene: CST3

Linked Data

• dbSNP Id: rs750555631
• gnomAD v4: 20-23637667-C-A
• MyVariant Identifiers: chr20:g.23618304C>A (hg19) ; chr20:g.23637667C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637667C>A , CM000682.2:g.23637667C>A	GRCh38
NC_000020.10:g.23618304C>A , CM000682.1:g.23618304C>A	GRCh37
NC_000020.9:g.23566304C>A	NCBI36
NG_012887.2:g.5271G>T
NG_012887.3:g.5271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.196G>T MANE Select	ENSP00000366124.3:p.Asp66Tyr
ENST00000376925.7:c.196G>T	ENSP00000366124.3:p.Asp66Tyr
ENST00000398409.1:c.196G>T	ENSP00000381446.1:p.Asp66Tyr
ENST00000398411.5:c.196G>T	ENSP00000381448.1:p.Asp66Tyr
NM_000099.3:c.196G>T	NP_000090.1:p.Asp66Tyr
NM_001288614.1:c.196G>T	NP_001275543.1:p.Asp66Tyr
NM_000099.4:c.196G>T MANE Select	NP_000090.1:p.Asp66Tyr
NM_001288614.2:c.196G>T	NP_001275543.1:p.Asp66Tyr