Canonical Allele Identifier: CA1657688851
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450147_117450151delinsCAACT , CM000668.2:g.117450147_117450151delinsCAACT GRCh38
NC_000006.11:g.117771310_117771314delinsCAACT , CM000668.1:g.117771310_117771314delinsCAACT GRCh37
NC_000006.10:g.117878003_117878007delinsCAACT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467125.1:c.547+116703_547+116707delinsAGTTG ENSP00000487717.1:n.547+116703_547+116707...