Canonical Allele Identifier: CA392615873

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1504C>A MANE Select	ENSP00000260408.3:p.Gln502Lys
ENST00000260408.7:c.1504C>A	ENSP00000260408.3:p.Gln502Lys
ENST00000396136.6:c.1330C>A
ENST00000402627.5:c.154+11837C>A	ENSP00000386056.1:n.154+11837C>A
ENST00000462061.1:n.64C>A
ENST00000470269.5:n.33C>A
ENST00000475898.1:n.529C>A
ENST00000481164.1:n.27C>A
ENST00000482945.5:n.27C>A
ENST00000561288.1:c.56-23960C>A	ENSP00000452639.1:n.56-23960C>A
NM_001110.3:c.1504C>A	NP_001101.1:p.Gln502Lys
XM_005254117.2:c.1411C>A	XP_005254174.1:p.Gln471Lys
NM_001320570.1:c.1411C>A	NP_001307499.1:p.Gln471Lys
XM_024449818.1:c.1282C>A	XP_024305586.1:p.Gln428Lys
NM_001110.4:c.1504C>A MANE Select	NP_001101.1:p.Gln502Lys
NM_001320570.2:c.1411C>A	NP_001307499.1:p.Gln471Lys