Canonical Allele Identifier: CA2180427110

Gene: ADAM10

Linked Data

• dbSNP Id: rs1595988347
• gnomAD v4: 15-58610713-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610713C>T , CM000677.2:g.58610713C>T	GRCh38
NC_000015.9:g.58902912C>T , CM000677.1:g.58902912C>T	GRCh37
NC_000015.8:g.56690204C>T	NCBI36
NG_033876.1:g.144266G>A
NG_033876.2:g.143995G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1805-196G>A MANE Select	ENSP00000260408.3:n.1805-196G>A
ENST00000260408.7:c.1805-196G>A	ENSP00000260408.3:n.1805-196G>A
ENST00000396136.6:c.1631-196G>A
ENST00000402627.5:c.155-13195G>A	ENSP00000386056.1:n.155-13195G>A
ENST00000470269.5:n.334-196G>A
ENST00000482945.5:n.1313G>A
ENST00000561288.1:c.56-13195G>A	ENSP00000452639.1:n.56-13195G>A
NM_001110.3:c.1805-196G>A	NP_001101.1:n.1805-196G>A
XM_005254117.2:c.1712-196G>A	XP_005254174.1:n.1712-196G>A
NM_001320570.1:c.1712-196G>A	NP_001307499.1:n.1712-196G>A
XM_024449818.1:c.1583-196G>A	XP_024305586.1:n.1583-196G>A
NM_001110.4:c.1805-196G>A MANE Select	NP_001101.1:n.1805-196G>A
NM_001320570.2:c.1712-196G>A	NP_001307499.1:n.1712-196G>A