Canonical Allele Identifier: CA2628687774

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58665068-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665071del , CM000677.2:g.58665071del	GRCh38
NC_000015.9:g.58957270del , CM000677.1:g.58957270del	GRCh37
NC_000015.8:g.56744562del	NCBI36
NG_033876.1:g.89910del
NG_033876.2:g.89639del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.585+28del MANE Select	ENSP00000260408.3:n.585+28del
ENST00000260408.7:c.585+28del	ENSP00000260408.3:n.585+28del
ENST00000396136.6:c.411+28del
ENST00000402627.5:c.56-24239del	ENSP00000386056.1:n.56-24239del
ENST00000558733.5:n.821+28del
ENST00000559053.1:c.56-24239del	ENSP00000453952.1:n.56-24239del
ENST00000561288.1:c.56-67551del	ENSP00000452639.1:n.56-67551del
NM_001110.3:c.585+28del	NP_001101.1:n.585+28del
XM_005254117.2:c.585+28del	XP_005254174.1:n.585+28del
NM_001320570.1:c.585+28del	NP_001307499.1:n.585+28del
XM_024449818.1:c.363+28del	XP_024305586.1:n.363+28del
NM_001110.4:c.585+28del MANE Select	NP_001101.1:n.585+28del
NM_001320570.2:c.585+28del	NP_001307499.1:n.585+28del