Canonical Allele Identifier: CA15856860

Gene: ADAM10

Linked Data

• dbSNP Id: rs347117
• gnomAD v2: 15-59000957-C-T
• gnomAD v3: 15-58708758-C-T
• gnomAD v4: 15-58708758-C-T
• MyVariant Identifiers: chr15:g.59000957C>T (hg19) ; chr15:g.58708758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58708758C>T , CM000677.2:g.58708758C>T	GRCh38
NC_000015.9:g.59000957C>T , CM000677.1:g.59000957C>T	GRCh37
NC_000015.8:g.56788249C>T	NCBI36
NG_033876.1:g.46221G>A
NG_033876.2:g.45950G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.206+8819G>A MANE Select	ENSP00000260408.3:n.206+8819G>A
ENST00000260408.7:c.206+8819G>A	ENSP00000260408.3:n.206+8819G>A
ENST00000402627.5:c.55+40722G>A	ENSP00000386056.1:n.55+40722G>A
ENST00000439637.5:c.206+8819G>A	ENSP00000391930.1:n.206+8819G>A
ENST00000497846.5:n.323+8819G>A
ENST00000558004.1:c.206+8819G>A	ENSP00000452704.1:n.206+8819G>A
ENST00000558733.5:n.442+8819G>A
ENST00000559053.1:c.55+40722G>A	ENSP00000453952.1:n.55+40722G>A
ENST00000560608.5:n.463+8819G>A
ENST00000561149.1:n.393-1378G>A
ENST00000561288.1:c.55+40722G>A	ENSP00000452639.1:n.55+40722G>A
NM_001110.3:c.206+8819G>A	NP_001101.1:n.206+8819G>A
XM_005254117.2:c.206+8819G>A	XP_005254174.1:n.206+8819G>A
NM_001320570.1:c.206+8819G>A	NP_001307499.1:n.206+8819G>A
XM_024449818.1:c.-17+8819G>A	XP_024305586.1:n.-17+8819G>A
NM_001110.4:c.206+8819G>A MANE Select	NP_001101.1:n.206+8819G>A
NM_001320570.2:c.206+8819G>A	NP_001307499.1:n.206+8819G>A