Canonical Allele Identifier: CA392621859

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957356A>C (hg19) ; chr15:g.58665157A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665157A>C , CM000677.2:g.58665157A>C	GRCh38
NC_000015.9:g.58957356A>C , CM000677.1:g.58957356A>C	GRCh37
NC_000015.8:g.56744648A>C	NCBI36
NG_033876.1:g.89822T>G
NG_033876.2:g.89551T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.525T>G MANE Select	ENSP00000260408.3:p.Asp175Glu
ENST00000260408.7:c.525T>G	ENSP00000260408.3:p.Asp175Glu
ENST00000396136.6:c.351T>G
ENST00000402627.5:c.56-24327T>G	ENSP00000386056.1:n.56-24327T>G
ENST00000439637.5:c.366T>G	ENSP00000391930.1:p.Asp122Glu
ENST00000497846.5:n.642T>G
ENST00000558733.5:n.761T>G
ENST00000559053.1:c.56-24327T>G	ENSP00000453952.1:n.56-24327T>G
ENST00000561288.1:c.56-67639T>G	ENSP00000452639.1:n.56-67639T>G
NM_001110.3:c.525T>G	NP_001101.1:p.Asp175Glu
XM_005254117.2:c.525T>G	XP_005254174.1:p.Asp175Glu
NM_001320570.1:c.525T>G	NP_001307499.1:p.Asp175Glu
XM_024449818.1:c.303T>G	XP_024305586.1:p.Asp101Glu
NM_001110.4:c.525T>G MANE Select	NP_001101.1:p.Asp175Glu
NM_001320570.2:c.525T>G	NP_001307499.1:p.Asp175Glu