Canonical Allele Identifier: CA2594039731

Gene: ADAM10

Linked Data

• gnomAD v3: 15-58610831-CATAATA-C
• gnomAD v4: 15-58610831-CATAATA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610835_58610840del , CM000677.2:g.58610835_58610840del	GRCh38
NC_000015.9:g.58903034_58903039del , CM000677.1:g.58903034_58903039del	GRCh37
NC_000015.8:g.56690326_56690331del	NCBI36
NG_033876.1:g.144142_144147del
NG_033876.2:g.143871_143876del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+162_1804+167del MANE Select	ENSP00000260408.3:n.1804+162_1804+167del
ENST00000260408.7:c.1804+162_1804+167del	ENSP00000260408.3:n.1804+162_1804+167del
ENST00000396136.6:c.1630+162_1630+167del
ENST00000402627.5:c.155-13319_155-13314del	ENSP00000386056.1:n.155-13319_155-13314del
ENST00000470269.5:n.333+162_333+167del
ENST00000482945.5:n.1189_1194del
ENST00000561288.1:c.56-13319_56-13314del	ENSP00000452639.1:n.56-13319_56-13314del
NM_001110.3:c.1804+162_1804+167del	NP_001101.1:n.1804+162_1804+167del
XM_005254117.2:c.1711+162_1711+167del	XP_005254174.1:n.1711+162_1711+167del
NM_001320570.1:c.1711+162_1711+167del	NP_001307499.1:n.1711+162_1711+167del
XM_024449818.1:c.1582+162_1582+167del	XP_024305586.1:n.1582+162_1582+167del
NM_001110.4:c.1804+162_1804+167del MANE Select	NP_001101.1:n.1804+162_1804+167del
NM_001320570.2:c.1711+162_1711+167del	NP_001307499.1:n.1711+162_1711+167del