Canonical Allele Identifier: CA1674885562
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812330_155812332delinsCTA , CM000668.2:g.155812330_155812332delinsCTA GRCh38
NC_000006.11:g.156133464_156133466delinsCTA , CM000668.1:g.156133464_156133466delinsCTA GRCh37
NC_000006.10:g.156175156_156175158delinsCTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18911_79+18913delinsCTA
XR_943146.1:n.645-293_645-291delinsTAG
XR_001744423.1:n.699-293_699-291delinsTAG
XR_001744424.1:n.79+18911_79+18913delinsCTA