Canonical Allele Identifier: CA2180485088
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58741862A= , CM000677.2:g.58741862A= GRCh38
NC_000015.9:g.59034061A= , CM000677.1:g.59034061A= GRCh37
NC_000015.8:g.56821353A= NCBI36
NG_033876.1:g.13117T=
NG_033876.2:g.12846T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260408.8:c.55+7618T= MANE Select ENSP00000260408.3:n.55+7618T=
ENST00000260408.7:c.55+7618T= ENSP00000260408.3:n.55+7618T=
ENST00000402627.5:c.55+7618T= ENSP00000386056.1:n.55+7618T=
ENST00000439637.5:c.55+7618T= ENSP00000391930.1:n.55+7618T=
ENST00000497846.5:n.172+6933T=
ENST00000558004.1:c.55+7618T= ENSP00000452704.1:n.55+7618T=
ENST00000558733.5:n.291+7618T=
ENST00000559053.1:c.55+7618T= ENSP00000453952.1:n.55+7618T=
ENST00000560608.5:n.312+7618T=
ENST00000561149.1:n.241+7618T=
ENST00000561288.1:c.55+7618T= ENSP00000452639.1:n.55+7618T=
NM_001110.3:c.55+7618T= NP_001101.1:n.55+7618T=
XM_005254117.2:c.55+7618T= XP_005254174.1:n.55+7618T=
NM_001320570.1:c.55+7618T= NP_001307499.1:n.55+7618T=
XM_024449818.1:c.-168+6933T= XP_024305586.1:n.-168+6933T=
NM_001110.4:c.55+7618T= MANE Select NP_001101.1:n.55+7618T=
NM_001320570.2:c.55+7618T= NP_001307499.1:n.55+7618T=