Canonical Allele Identifier: CA2628685381
Gene: ADAM10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58610797G>T , CM000677.2:g.58610797G>T GRCh38
NC_000015.9:g.58902996G>T , CM000677.1:g.58902996G>T GRCh37
NC_000015.8:g.56690288G>T NCBI36
NG_033876.1:g.144182C>A
NG_033876.2:g.143911C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260408.8:c.1804+202C>A MANE Select ENSP00000260408.3:n.1804+202C>A
ENST00000260408.7:c.1804+202C>A ENSP00000260408.3:n.1804+202C>A
ENST00000396136.6:c.1630+202C>A
ENST00000402627.5:c.155-13279C>A ENSP00000386056.1:n.155-13279C>A
ENST00000470269.5:n.333+202C>A
ENST00000482945.5:n.1229C>A
ENST00000561288.1:c.56-13279C>A ENSP00000452639.1:n.56-13279C>A
NM_001110.3:c.1804+202C>A NP_001101.1:n.1804+202C>A
XM_005254117.2:c.1711+202C>A XP_005254174.1:n.1711+202C>A
NM_001320570.1:c.1711+202C>A NP_001307499.1:n.1711+202C>A
XM_024449818.1:c.1582+202C>A XP_024305586.1:n.1582+202C>A
NM_001110.4:c.1804+202C>A MANE Select NP_001101.1:n.1804+202C>A
NM_001320570.2:c.1711+202C>A NP_001307499.1:n.1711+202C>A