Canonical Allele Identifier: CA2180427121
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58610733T= , CM000677.2:g.58610733T= GRCh38
NC_000015.9:g.58902932T= , CM000677.1:g.58902932T= GRCh37
NC_000015.8:g.56690224T= NCBI36
NG_033876.1:g.144246A=
NG_033876.2:g.143975A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.8:c.1805-216A= MANE Select ENSP00000260408.3:n.1805-216A=
ENST00000260408.7:c.1805-216A= ENSP00000260408.3:n.1805-216A=
ENST00000396136.6:c.1631-216A=
ENST00000402627.5:c.155-13215A= ENSP00000386056.1:n.155-13215A=
ENST00000470269.5:n.334-216A=
ENST00000482945.5:n.1293A=
ENST00000561288.1:c.56-13215A= ENSP00000452639.1:n.56-13215A=
NM_001110.3:c.1805-216A= NP_001101.1:n.1805-216A=
XM_005254117.2:c.1712-216A= XP_005254174.1:n.1712-216A=
NM_001320570.1:c.1712-216A= NP_001307499.1:n.1712-216A=
XM_024449818.1:c.1583-216A= XP_024305586.1:n.1583-216A=
NM_001110.4:c.1805-216A= MANE Select NP_001101.1:n.1805-216A=
NM_001320570.2:c.1712-216A= NP_001307499.1:n.1712-216A=