Canonical Allele Identifier: CA392615872

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1504C>T MANE Select	ENSP00000260408.3:p.Gln502Ter
ENST00000260408.7:c.1504C>T	ENSP00000260408.3:p.Gln502Ter
ENST00000396136.6:c.1330C>T
ENST00000402627.5:c.154+11837C>T	ENSP00000386056.1:n.154+11837C>T
ENST00000462061.1:n.64C>T
ENST00000470269.5:n.33C>T
ENST00000475898.1:n.529C>T
ENST00000481164.1:n.27C>T
ENST00000482945.5:n.27C>T
ENST00000561288.1:c.56-23960C>T	ENSP00000452639.1:n.56-23960C>T
NM_001110.3:c.1504C>T	NP_001101.1:p.Gln502Ter
XM_005254117.2:c.1411C>T	XP_005254174.1:p.Gln471Ter
NM_001320570.1:c.1411C>T	NP_001307499.1:p.Gln471Ter
XM_024449818.1:c.1282C>T	XP_024305586.1:p.Gln428Ter
NM_001110.4:c.1504C>T MANE Select	NP_001101.1:p.Gln502Ter
NM_001320570.2:c.1411C>T	NP_001307499.1:p.Gln471Ter