Canonical Allele Identifier: CA1168497153

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56262306_56262307delinsTG , CM000663.2:g.56262306_56262307delinsTG	GRCh38
NC_000001.10:g.56727978_56727979delinsTG , CM000663.1:g.56727978_56727979delinsTG	GRCh37
NC_000001.9:g.56500566_56500567delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641109.1:c.760-13107_760-13106delinsCA	ENSP00000493138.1:n.760-13107_760-13106delinsCA
ENST00000641346.1:c.367-13107_367-13106delinsCA
ENST00000641415.1:c.193-8414_193-8413delinsCA
ENST00000641494.1:c.379-13107_379-13106delinsCA
ENST00000642129.1:c.769-13107_769-13106delinsCA