Canonical Allele Identifier: CA2180493314
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749969C= , CM000677.2:g.58749969C= GRCh38
NC_000015.9:g.59042168C= , CM000677.1:g.59042168C= GRCh37
NC_000015.8:g.56829460C= NCBI36
NG_033876.1:g.5010G=
NG_033876.2:g.4739G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-435G= ENSP00000260408.3:n.-435G=
NM_001110.3:c.-435G= NP_001101.1:n.-435G=
NM_001320570.1:c.-435G= NP_001307499.1:n.-435G=