Canonical Allele Identifier: CA392621874

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957358C>G (hg19) ; chr15:g.58665159C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665159C>G , CM000677.2:g.58665159C>G	GRCh38
NC_000015.9:g.58957358C>G , CM000677.1:g.58957358C>G	GRCh37
NC_000015.8:g.56744650C>G	NCBI36
NG_033876.1:g.89820G>C
NG_033876.2:g.89549G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.523G>C MANE Select	ENSP00000260408.3:p.Asp175His
ENST00000260408.7:c.523G>C	ENSP00000260408.3:p.Asp175His
ENST00000396136.6:c.349G>C
ENST00000402627.5:c.56-24329G>C	ENSP00000386056.1:n.56-24329G>C
ENST00000439637.5:c.364G>C	ENSP00000391930.1:p.Asp122His
ENST00000497846.5:n.640G>C
ENST00000558733.5:n.759G>C
ENST00000559053.1:c.56-24329G>C	ENSP00000453952.1:n.56-24329G>C
ENST00000561288.1:c.56-67641G>C	ENSP00000452639.1:n.56-67641G>C
NM_001110.3:c.523G>C	NP_001101.1:p.Asp175His
XM_005254117.2:c.523G>C	XP_005254174.1:p.Asp175His
NM_001320570.1:c.523G>C	NP_001307499.1:p.Asp175His
XM_024449818.1:c.301G>C	XP_024305586.1:p.Asp101His
NM_001110.4:c.523G>C MANE Select	NP_001101.1:p.Asp175His
NM_001320570.2:c.523G>C	NP_001307499.1:p.Asp175His