Canonical Allele Identifier: CA2628687775

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58665071-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665071A>G , CM000677.2:g.58665071A>G	GRCh38
NC_000015.9:g.58957270A>G , CM000677.1:g.58957270A>G	GRCh37
NC_000015.8:g.56744562A>G	NCBI36
NG_033876.1:g.89908T>C
NG_033876.2:g.89637T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.585+26T>C MANE Select	ENSP00000260408.3:n.585+26T>C
ENST00000260408.7:c.585+26T>C	ENSP00000260408.3:n.585+26T>C
ENST00000396136.6:c.411+26T>C
ENST00000402627.5:c.56-24241T>C	ENSP00000386056.1:n.56-24241T>C
ENST00000558733.5:n.821+26T>C
ENST00000559053.1:c.56-24241T>C	ENSP00000453952.1:n.56-24241T>C
ENST00000561288.1:c.56-67553T>C	ENSP00000452639.1:n.56-67553T>C
NM_001110.3:c.585+26T>C	NP_001101.1:n.585+26T>C
XM_005254117.2:c.585+26T>C	XP_005254174.1:n.585+26T>C
NM_001320570.1:c.585+26T>C	NP_001307499.1:n.585+26T>C
XM_024449818.1:c.363+26T>C	XP_024305586.1:n.363+26T>C
NM_001110.4:c.585+26T>C MANE Select	NP_001101.1:n.585+26T>C
NM_001320570.2:c.585+26T>C	NP_001307499.1:n.585+26T>C