Canonical Allele Identifier: CA392621913

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957364A>G (hg19) ; chr15:g.58665165A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665165A>G , CM000677.2:g.58665165A>G	GRCh38
NC_000015.9:g.58957364A>G , CM000677.1:g.58957364A>G	GRCh37
NC_000015.8:g.56744656A>G	NCBI36
NG_033876.1:g.89814T>C
NG_033876.2:g.89543T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.517T>C MANE Select	ENSP00000260408.3:p.Cys173Arg
ENST00000260408.7:c.517T>C	ENSP00000260408.3:p.Cys173Arg
ENST00000396136.6:c.343T>C
ENST00000402627.5:c.56-24335T>C	ENSP00000386056.1:n.56-24335T>C
ENST00000439637.5:c.358T>C	ENSP00000391930.1:p.Cys120Arg
ENST00000497846.5:n.634T>C
ENST00000558733.5:n.753T>C
ENST00000559053.1:c.56-24335T>C	ENSP00000453952.1:n.56-24335T>C
ENST00000561288.1:c.56-67647T>C	ENSP00000452639.1:n.56-67647T>C
NM_001110.3:c.517T>C	NP_001101.1:p.Cys173Arg
XM_005254117.2:c.517T>C	XP_005254174.1:p.Cys173Arg
NM_001320570.1:c.517T>C	NP_001307499.1:p.Cys173Arg
XM_024449818.1:c.295T>C	XP_024305586.1:p.Cys99Arg
NM_001110.4:c.517T>C MANE Select	NP_001101.1:p.Cys173Arg
NM_001320570.2:c.517T>C	NP_001307499.1:p.Cys173Arg