Canonical Allele Identifier: CA392615874

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913677G>C (hg19) ; chr15:g.58621478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621478G>C , CM000677.2:g.58621478G>C	GRCh38
NC_000015.9:g.58913677G>C , CM000677.1:g.58913677G>C	GRCh37
NC_000015.8:g.56700969G>C	NCBI36
NG_033876.1:g.133501C>G
NG_033876.2:g.133230C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1504C>G MANE Select	ENSP00000260408.3:p.Gln502Glu
ENST00000260408.7:c.1504C>G	ENSP00000260408.3:p.Gln502Glu
ENST00000396136.6:c.1330C>G
ENST00000402627.5:c.154+11837C>G	ENSP00000386056.1:n.154+11837C>G
ENST00000462061.1:n.64C>G
ENST00000470269.5:n.33C>G
ENST00000475898.1:n.529C>G
ENST00000481164.1:n.27C>G
ENST00000482945.5:n.27C>G
ENST00000561288.1:c.56-23960C>G	ENSP00000452639.1:n.56-23960C>G
NM_001110.3:c.1504C>G	NP_001101.1:p.Gln502Glu
XM_005254117.2:c.1411C>G	XP_005254174.1:p.Gln471Glu
NM_001320570.1:c.1411C>G	NP_001307499.1:p.Gln471Glu
XM_024449818.1:c.1282C>G	XP_024305586.1:p.Gln428Glu
NM_001110.4:c.1504C>G MANE Select	NP_001101.1:p.Gln502Glu
NM_001320570.2:c.1411C>G	NP_001307499.1:p.Gln471Glu