Canonical Allele Identifier: CA392621857

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957355G>T (hg19) ; chr15:g.58665156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665156G>T , CM000677.2:g.58665156G>T	GRCh38
NC_000015.9:g.58957355G>T , CM000677.1:g.58957355G>T	GRCh37
NC_000015.8:g.56744647G>T	NCBI36
NG_033876.1:g.89823C>A
NG_033876.2:g.89552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.526C>A MANE Select	ENSP00000260408.3:p.His176Asn
ENST00000260408.7:c.526C>A	ENSP00000260408.3:p.His176Asn
ENST00000396136.6:c.352C>A
ENST00000402627.5:c.56-24326C>A	ENSP00000386056.1:n.56-24326C>A
ENST00000439637.5:c.367C>A	ENSP00000391930.1:p.His123Asn
ENST00000497846.5:n.643C>A
ENST00000558733.5:n.762C>A
ENST00000559053.1:c.56-24326C>A	ENSP00000453952.1:n.56-24326C>A
ENST00000561288.1:c.56-67638C>A	ENSP00000452639.1:n.56-67638C>A
NM_001110.3:c.526C>A	NP_001101.1:p.His176Asn
XM_005254117.2:c.526C>A	XP_005254174.1:p.His176Asn
NM_001320570.1:c.526C>A	NP_001307499.1:p.His176Asn
XM_024449818.1:c.304C>A	XP_024305586.1:p.His102Asn
NM_001110.4:c.526C>A MANE Select	NP_001101.1:p.His176Asn
NM_001320570.2:c.526C>A	NP_001307499.1:p.His176Asn