Canonical Allele Identifier: CA2652171749

Gene: CST3

Linked Data

• gnomAD v4: 20-23637615-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637615C>A , CM000682.2:g.23637615C>A	GRCh38
NC_000020.10:g.23618252C>A , CM000682.1:g.23618252C>A	GRCh37
NC_000020.9:g.23566252C>A	NCBI36
NG_012887.2:g.5323G>T
NG_012887.3:g.5323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.243+5G>T MANE Select	ENSP00000366124.3:n.243+5G>T
ENST00000376925.7:c.243+5G>T	ENSP00000366124.3:n.243+5G>T
ENST00000398409.1:c.243+5G>T	ENSP00000381446.1:n.243+5G>T
ENST00000398411.5:c.243+5G>T	ENSP00000381448.1:n.243+5G>T
NM_000099.3:c.243+5G>T	NP_000090.1:n.243+5G>T
NM_001288614.1:c.243+5G>T	NP_001275543.1:n.243+5G>T
NM_000099.4:c.243+5G>T MANE Select	NP_000090.1:n.243+5G>T
NM_001288614.2:c.243+5G>T	NP_001275543.1:n.243+5G>T