Canonical Allele Identifier: CA7585711

Gene: ADAM10

Linked Data

• dbSNP Id: rs371036827
• ExAC: 15:58957358 C / T
• gnomAD v2: 15-58957358-C-T
• gnomAD v3: 15-58665159-C-T
• gnomAD v4: 15-58665159-C-T
• MyVariant Identifiers: chr15:g.58957358C>T (hg19) ; chr15:g.58665159C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665159C>T , CM000677.2:g.58665159C>T	GRCh38
NC_000015.9:g.58957358C>T , CM000677.1:g.58957358C>T	GRCh37
NC_000015.8:g.56744650C>T	NCBI36
NG_033876.1:g.89820G>A
NG_033876.2:g.89549G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.523G>A MANE Select	ENSP00000260408.3:p.Asp175Asn
ENST00000260408.7:c.523G>A	ENSP00000260408.3:p.Asp175Asn
ENST00000396136.6:c.349G>A
ENST00000402627.5:c.56-24329G>A	ENSP00000386056.1:n.56-24329G>A
ENST00000439637.5:c.364G>A	ENSP00000391930.1:p.Asp122Asn
ENST00000497846.5:n.640G>A
ENST00000558733.5:n.759G>A
ENST00000559053.1:c.56-24329G>A	ENSP00000453952.1:n.56-24329G>A
ENST00000561288.1:c.56-67641G>A	ENSP00000452639.1:n.56-67641G>A
NM_001110.3:c.523G>A	NP_001101.1:p.Asp175Asn
XM_005254117.2:c.523G>A	XP_005254174.1:p.Asp175Asn
NM_001320570.1:c.523G>A	NP_001307499.1:p.Asp175Asn
XM_024449818.1:c.301G>A	XP_024305586.1:p.Asp101Asn
NM_001110.4:c.523G>A MANE Select	NP_001101.1:p.Asp175Asn
NM_001320570.2:c.523G>A	NP_001307499.1:p.Asp175Asn