Canonical Allele Identifier: CA490492321

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957365G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665166G>T , CM000677.2:g.58665166G>T	GRCh38
NC_000015.9:g.58957365G>T , CM000677.1:g.58957365G>T	GRCh37
NC_000015.8:g.56744657G>T	NCBI36
NG_033876.1:g.89813C>A
NG_033876.2:g.89542C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.516C>A MANE Select	ENSP00000260408.3:p.Gly172=
ENST00000260408.7:c.516C>A	ENSP00000260408.3:p.Gly172=
ENST00000396136.6:c.342C>A
ENST00000402627.5:c.56-24336C>A	ENSP00000386056.1:n.56-24336C>A
ENST00000439637.5:c.357C>A	ENSP00000391930.1:p.Gly119=
ENST00000497846.5:n.633C>A
ENST00000558733.5:n.752C>A
ENST00000559053.1:c.56-24336C>A	ENSP00000453952.1:n.56-24336C>A
ENST00000561288.1:c.56-67648C>A	ENSP00000452639.1:n.56-67648C>A
NM_001110.3:c.516C>A	NP_001101.1:p.Gly172=
XM_005254117.2:c.516C>A	XP_005254174.1:p.Gly172=
NM_001320570.1:c.516C>A	NP_001307499.1:p.Gly172=
XM_024449818.1:c.294C>A	XP_024305586.1:p.Gly98=
NM_001110.4:c.516C>A MANE Select	NP_001101.1:p.Gly172=
NM_001320570.2:c.516C>A	NP_001307499.1:p.Gly172=