Canonical Allele Identifier: CA490493708

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913678T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621479T>C , CM000677.2:g.58621479T>C	GRCh38
NC_000015.9:g.58913678T>C , CM000677.1:g.58913678T>C	GRCh37
NC_000015.8:g.56700970T>C	NCBI36
NG_033876.1:g.133500A>G
NG_033876.2:g.133229A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1503A>G MANE Select	ENSP00000260408.3:p.Lys501=
ENST00000260408.7:c.1503A>G	ENSP00000260408.3:p.Lys501=
ENST00000396136.6:c.1329A>G
ENST00000402627.5:c.154+11836A>G	ENSP00000386056.1:n.154+11836A>G
ENST00000462061.1:n.63A>G
ENST00000470269.5:n.32A>G
ENST00000475898.1:n.528A>G
ENST00000481164.1:n.26A>G
ENST00000482945.5:n.26A>G
ENST00000561288.1:c.56-23961A>G	ENSP00000452639.1:n.56-23961A>G
NM_001110.3:c.1503A>G	NP_001101.1:p.Lys501=
XM_005254117.2:c.1410A>G	XP_005254174.1:p.Lys470=
NM_001320570.1:c.1410A>G	NP_001307499.1:p.Lys470=
XM_024449818.1:c.1281A>G	XP_024305586.1:p.Lys427=
NM_001110.4:c.1503A>G MANE Select	NP_001101.1:p.Lys501=
NM_001320570.2:c.1410A>G	NP_001307499.1:p.Lys470=