Canonical Allele Identifier: CA2180493319
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749971G= , CM000677.2:g.58749971G= GRCh38
NC_000015.9:g.59042170G= , CM000677.1:g.59042170G= GRCh37
NC_000015.8:g.56829462G= NCBI36
NG_033876.1:g.5008C=
NG_033876.2:g.4737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-437C= ENSP00000260408.3:n.-437C=
NM_001110.3:c.-437C= NP_001101.1:n.-437C=
NM_001320570.1:c.-437C= NP_001307499.1:n.-437C=