Canonical Allele Identifier: CA1841175617
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551490_25551492delinsCTG , CM000671.2:g.25551490_25551492delinsCTG GRCh38
NC_000009.11:g.25551488_25551490delinsCTG , CM000671.1:g.25551488_25551490delinsCTG GRCh37
NC_000009.10:g.25541488_25541490delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-920_50-918delinsCAG
XR_929525.2:n.674-920_674-918delinsCAG