Canonical Allele Identifier: CA2180432532
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58621406_58621408delinsATT , CM000677.2:g.58621406_58621408delinsATT GRCh38
NC_000015.9:g.58913605_58913607delinsATT , CM000677.1:g.58913605_58913607delinsATT GRCh37
NC_000015.8:g.56700897_56700899delinsATT NCBI36
NG_033876.1:g.133571_133573delinsAAT
NG_033876.2:g.133300_133302delinsAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000260408.8:c.1511+63_1511+65delinsAAT MANE Select ENSP00000260408.3:n.1511+63_1511+65delins...
ENST00000260408.7:c.1511+63_1511+65delinsAAT ENSP00000260408.3:n.1511+63_1511+65delins...
ENST00000396136.6:c.1337+63_1337+65delinsAAT
ENST00000402627.5:c.154+11907_154+11909delinsAAT ENSP00000386056.1:n.154+11907_154+11909de...
ENST00000462061.1:n.71+63_71+65delinsAAT
ENST00000470269.5:n.40+63_40+65delinsAAT
ENST00000475898.1:n.536+63_536+65delinsAAT
ENST00000481164.1:n.34+63_34+65delinsAAT
ENST00000482945.5:n.34+63_34+65delinsAAT
ENST00000561288.1:c.56-23890_56-23888delinsAAT ENSP00000452639.1:n.56-23890_56-23888deli...
NM_001110.3:c.1511+63_1511+65delinsAAT NP_001101.1:n.1511+63_1511+65delinsAAT
XM_005254117.2:c.1418+63_1418+65delinsAAT XP_005254174.1:n.1418+63_1418+65delinsAAT...
NM_001320570.1:c.1418+63_1418+65delinsAAT NP_001307499.1:n.1418+63_1418+65delinsAAT...
XM_024449818.1:c.1289+63_1289+65delinsAAT XP_024305586.1:n.1289+63_1289+65delinsAAT...
NM_001110.4:c.1511+63_1511+65delinsAAT MANE Select NP_001101.1:n.1511+63_1511+65delinsAAT
NM_001320570.2:c.1418+63_1418+65delinsAAT NP_001307499.1:n.1418+63_1418+65delinsAAT...