Canonical Allele Identifier: CA1941455898

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458276_122458278delinsCCG , CM000672.2:g.122458276_122458278delinsCCG	GRCh38
NC_000010.10:g.124217792_124217794delinsCCG , CM000672.1:g.124217792_124217794delinsCCG	GRCh37
NC_000010.9:g.124207782_124207784delinsCCG	NCBI36
NG_011554.1:g.1752_1754delinsCCG
NG_011725.1:g.8614_8616delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+217_1827+219delinsCGG
XR_946383.1:n.1827+217_1827+219delinsCGG
XR_946384.1:n.1576+217_1576+219delinsCGG
XR_946385.1:n.1827+217_1827+219delinsCGG
XR_946382.2:n.1855+217_1855+219delinsCGG
XR_946383.2:n.1855+217_1855+219delinsCGG
XR_946384.2:n.1580+217_1580+219delinsCGG
XR_946385.2:n.1855+217_1855+219delinsCGG