Canonical Allele Identifier: CA2180493211
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749925G= , CM000677.2:g.58749925G= GRCh38
NC_000015.9:g.59042124G= , CM000677.1:g.59042124G= GRCh37
NC_000015.8:g.56829416G= NCBI36
NG_033876.1:g.5054C=
NG_033876.2:g.4783C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-391C= ENSP00000260408.3:n.-391C=
NM_001110.3:c.-391C= NP_001101.1:n.-391C=
NM_001320570.1:c.-391C= NP_001307499.1:n.-391C=