Canonical Allele Identifier: CA714332508

Gene: ADAM10

Linked Data

• dbSNP Id: rs1302345595
• gnomAD v3: 15-58708711-A-C
• gnomAD v4: 15-58708711-A-C
• MyVariant Identifiers: chr15:g.59000910A>C (hg19) ; chr15:g.58708711A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58708711A>C , CM000677.2:g.58708711A>C	GRCh38
NC_000015.9:g.59000910A>C , CM000677.1:g.59000910A>C	GRCh37
NC_000015.8:g.56788202A>C	NCBI36
NG_033876.1:g.46268T>G
NG_033876.2:g.45997T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.206+8866T>G MANE Select	ENSP00000260408.3:n.206+8866T>G
ENST00000260408.7:c.206+8866T>G	ENSP00000260408.3:n.206+8866T>G
ENST00000402627.5:c.55+40769T>G	ENSP00000386056.1:n.55+40769T>G
ENST00000439637.5:c.206+8866T>G	ENSP00000391930.1:n.206+8866T>G
ENST00000497846.5:n.323+8866T>G
ENST00000558004.1:c.206+8866T>G	ENSP00000452704.1:n.206+8866T>G
ENST00000558733.5:n.442+8866T>G
ENST00000559053.1:c.55+40769T>G	ENSP00000453952.1:n.55+40769T>G
ENST00000560608.5:n.463+8866T>G
ENST00000561149.1:n.393-1331T>G
ENST00000561288.1:c.55+40769T>G	ENSP00000452639.1:n.55+40769T>G
NM_001110.3:c.206+8866T>G	NP_001101.1:n.206+8866T>G
XM_005254117.2:c.206+8866T>G	XP_005254174.1:n.206+8866T>G
NM_001320570.1:c.206+8866T>G	NP_001307499.1:n.206+8866T>G
XM_024449818.1:c.-17+8866T>G	XP_024305586.1:n.-17+8866T>G
NM_001110.4:c.206+8866T>G MANE Select	NP_001101.1:n.206+8866T>G
NM_001320570.2:c.206+8866T>G	NP_001307499.1:n.206+8866T>G