Canonical Allele Identifier: CA1760508005

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907710_5907712delinsGAA , CM000670.2:g.5907710_5907712delinsGAA	GRCh38
NC_000008.10:g.5765232_5765234delinsGAA , CM000670.1:g.5765232_5765234delinsGAA	GRCh37
NC_000008.9:g.5752640_5752642delinsGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7981_308-7979delinsTTC
XR_941375.1:n.308-7981_308-7979delinsTTC
XR_941376.1:n.406-7981_406-7979delinsTTC
XR_941377.1:n.308-7981_308-7979delinsTTC
XR_941378.1:n.216-7981_216-7979delinsTTC
XR_001745765.1:n.308-7981_308-7979delinsTTC
XR_001745766.1:n.406-7981_406-7979delinsTTC
XR_001745767.1:n.216-7981_216-7979delinsTTC
XR_001745768.1:n.308-7981_308-7979delinsTTC
XR_941374.2:n.308-7981_308-7979delinsTTC
XR_941375.2:n.308-7981_308-7979delinsTTC