Canonical Allele Identifier: CA1760507782

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907464_5907468delinsCATAA , CM000670.2:g.5907464_5907468delinsCATAA	GRCh38
NC_000008.10:g.5764986_5764990delinsCATAA , CM000670.1:g.5764986_5764990delinsCATAA	GRCh37
NC_000008.9:g.5752394_5752398delinsCATAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7737_308-7733delinsTTATG
XR_941375.1:n.308-7737_308-7733delinsTTATG
XR_941376.1:n.406-7737_406-7733delinsTTATG
XR_941377.1:n.308-7737_308-7733delinsTTATG
XR_941378.1:n.216-7737_216-7733delinsTTATG
XR_001745765.1:n.308-7737_308-7733delinsTTATG
XR_001745766.1:n.406-7737_406-7733delinsTTATG
XR_001745767.1:n.216-7737_216-7733delinsTTATG
XR_001745768.1:n.308-7737_308-7733delinsTTATG
XR_941374.2:n.308-7737_308-7733delinsTTATG
XR_941375.2:n.308-7737_308-7733delinsTTATG