Canonical Allele Identifier: CA1760507482

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907110_5907112delinsTCA , CM000670.2:g.5907110_5907112delinsTCA	GRCh38
NC_000008.10:g.5764632_5764634delinsTCA , CM000670.1:g.5764632_5764634delinsTCA	GRCh37
NC_000008.9:g.5752040_5752042delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7381_308-7379delinsTGA
XR_941375.1:n.308-7381_308-7379delinsTGA
XR_941376.1:n.406-7381_406-7379delinsTGA
XR_941377.1:n.308-7381_308-7379delinsTGA
XR_941378.1:n.216-7381_216-7379delinsTGA
XR_001745765.1:n.308-7381_308-7379delinsTGA
XR_001745766.1:n.406-7381_406-7379delinsTGA
XR_001745767.1:n.216-7381_216-7379delinsTGA
XR_001745768.1:n.308-7381_308-7379delinsTGA
XR_941374.2:n.308-7381_308-7379delinsTGA
XR_941375.2:n.308-7381_308-7379delinsTGA