Canonical Allele Identifier: CA2628685396

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610839-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610840dup , CM000677.2:g.58610840dup	GRCh38
NC_000015.9:g.58903039dup , CM000677.1:g.58903039dup	GRCh37
NC_000015.8:g.56690331dup	NCBI36
NG_033876.1:g.144139dup
NG_033876.2:g.143868dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+159dup MANE Select	ENSP00000260408.3:n.1804+159dup
ENST00000260408.7:c.1804+159dup	ENSP00000260408.3:n.1804+159dup
ENST00000396136.6:c.1630+159dup
ENST00000402627.5:c.155-13322dup	ENSP00000386056.1:n.155-13322dup
ENST00000470269.5:n.333+159dup
ENST00000482945.5:n.1186dup
ENST00000561288.1:c.56-13322dup	ENSP00000452639.1:n.56-13322dup
NM_001110.3:c.1804+159dup	NP_001101.1:n.1804+159dup
XM_005254117.2:c.1711+159dup	XP_005254174.1:n.1711+159dup
NM_001320570.1:c.1711+159dup	NP_001307499.1:n.1711+159dup
XM_024449818.1:c.1582+159dup	XP_024305586.1:n.1582+159dup
NM_001110.4:c.1804+159dup MANE Select	NP_001101.1:n.1804+159dup
NM_001320570.2:c.1711+159dup	NP_001307499.1:n.1711+159dup