Canonical Allele Identifier: CA2180493201
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749923_58749924delinsAG , CM000677.2:g.58749923_58749924delinsAG GRCh38
NC_000015.9:g.59042122_59042123delinsAG , CM000677.1:g.59042122_59042123delinsAG GRCh37
NC_000015.8:g.56829414_56829415delinsAG NCBI36
NG_033876.1:g.5055_5056delinsCT
NG_033876.2:g.4784_4785delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-390_-389delinsCT ENSP00000260408.3:n.-390_-389delinsCT
NM_001110.3:c.-390_-389delinsCT NP_001101.1:n.-390_-389delinsCT
NM_001320570.1:c.-390_-389delinsCT NP_001307499.1:n.-390_-389delinsCT