Canonical Allele Identifier: CA2180485068
Gene: ADAM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58741832T= , CM000677.2:g.58741832T= GRCh38
NC_000015.9:g.59034031T= , CM000677.1:g.59034031T= GRCh37
NC_000015.8:g.56821323T= NCBI36
NG_033876.1:g.13147A=
NG_033876.2:g.12876A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260408.8:c.55+7648A= MANE Select ENSP00000260408.3:n.55+7648A=
ENST00000260408.7:c.55+7648A= ENSP00000260408.3:n.55+7648A=
ENST00000402627.5:c.55+7648A= ENSP00000386056.1:n.55+7648A=
ENST00000439637.5:c.55+7648A= ENSP00000391930.1:n.55+7648A=
ENST00000497846.5:n.172+6963A=
ENST00000558004.1:c.55+7648A= ENSP00000452704.1:n.55+7648A=
ENST00000558733.5:n.291+7648A=
ENST00000559053.1:c.55+7648A= ENSP00000453952.1:n.55+7648A=
ENST00000560608.5:n.312+7648A=
ENST00000561149.1:n.241+7648A=
ENST00000561288.1:c.55+7648A= ENSP00000452639.1:n.55+7648A=
NM_001110.3:c.55+7648A= NP_001101.1:n.55+7648A=
XM_005254117.2:c.55+7648A= XP_005254174.1:n.55+7648A=
NM_001320570.1:c.55+7648A= NP_001307499.1:n.55+7648A=
XM_024449818.1:c.-168+6963A= XP_024305586.1:n.-168+6963A=
NM_001110.4:c.55+7648A= MANE Select NP_001101.1:n.55+7648A=
NM_001320570.2:c.55+7648A= NP_001307499.1:n.55+7648A=