Canonical Allele Identifier: CA2355967041
Gene: CST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637616_23637617delinsGC , CM000682.2:g.23637616_23637617delinsGC GRCh38
NC_000020.10:g.23618253_23618254delinsGC , CM000682.1:g.23618253_23618254delinsGC GRCh37
NC_000020.9:g.23566253_23566254delinsGC NCBI36
NG_012887.2:g.5321_5322delinsGC
NG_012887.3:g.5321_5322delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.243+3_243+4delinsGC MANE Select ENSP00000366124.3:n.243+3_243+4delinsGC
ENST00000376925.7:c.243+3_243+4delinsGC ENSP00000366124.3:n.243+3_243+4delinsGC
ENST00000398409.1:c.243+3_243+4delinsGC ENSP00000381446.1:n.243+3_243+4delinsGC
ENST00000398411.5:c.243+3_243+4delinsGC ENSP00000381448.1:n.243+3_243+4delinsGC
NM_000099.3:c.243+3_243+4delinsGC NP_000090.1:n.243+3_243+4delinsGC
NM_001288614.1:c.243+3_243+4delinsGC NP_001275543.1:n.243+3_243+4delinsGC
NM_000099.4:c.243+3_243+4delinsGC MANE Select NP_000090.1:n.243+3_243+4delinsGC
NM_001288614.2:c.243+3_243+4delinsGC NP_001275543.1:n.243+3_243+4delinsGC