Canonical Allele Identifier: CA2180476222

Gene: ADAM10

Linked Data

• dbSNP Id: rs1897047923

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665050A>C , CM000677.2:g.58665050A>C	GRCh38
NC_000015.9:g.58957249A>C , CM000677.1:g.58957249A>C	GRCh37
NC_000015.8:g.56744541A>C	NCBI36
NG_033876.1:g.89929T>G
NG_033876.2:g.89658T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+47T>G MANE Select	ENSP00000260408.3:n.585+47T>G
ENST00000260408.7:c.585+47T>G	ENSP00000260408.3:n.585+47T>G
ENST00000396136.6:c.411+47T>G
ENST00000402627.5:c.56-24220T>G	ENSP00000386056.1:n.56-24220T>G
ENST00000558733.5:n.821+47T>G
ENST00000559053.1:c.56-24220T>G	ENSP00000453952.1:n.56-24220T>G
ENST00000561288.1:c.56-67532T>G	ENSP00000452639.1:n.56-67532T>G
NM_001110.3:c.585+47T>G	NP_001101.1:n.585+47T>G
XM_005254117.2:c.585+47T>G	XP_005254174.1:n.585+47T>G
NM_001320570.1:c.585+47T>G	NP_001307499.1:n.585+47T>G
XM_024449818.1:c.363+47T>G	XP_024305586.1:n.363+47T>G
NM_001110.4:c.585+47T>G MANE Select	NP_001101.1:n.585+47T>G
NM_001320570.2:c.585+47T>G	NP_001307499.1:n.585+47T>G