Canonical Allele Identifier: CA490492318

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957359T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665160T>A , CM000677.2:g.58665160T>A	GRCh38
NC_000015.9:g.58957359T>A , CM000677.1:g.58957359T>A	GRCh37
NC_000015.8:g.56744651T>A	NCBI36
NG_033876.1:g.89819A>T
NG_033876.2:g.89548A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.522A>T MANE Select	ENSP00000260408.3:p.Ala174=
ENST00000260408.7:c.522A>T	ENSP00000260408.3:p.Ala174=
ENST00000396136.6:c.348A>T
ENST00000402627.5:c.56-24330A>T	ENSP00000386056.1:n.56-24330A>T
ENST00000439637.5:c.363A>T	ENSP00000391930.1:p.Ala121=
ENST00000497846.5:n.639A>T
ENST00000558733.5:n.758A>T
ENST00000559053.1:c.56-24330A>T	ENSP00000453952.1:n.56-24330A>T
ENST00000561288.1:c.56-67642A>T	ENSP00000452639.1:n.56-67642A>T
NM_001110.3:c.522A>T	NP_001101.1:p.Ala174=
XM_005254117.2:c.522A>T	XP_005254174.1:p.Ala174=
NM_001320570.1:c.522A>T	NP_001307499.1:p.Ala174=
XM_024449818.1:c.300A>T	XP_024305586.1:p.Ala100=
NM_001110.4:c.522A>T MANE Select	NP_001101.1:p.Ala174=
NM_001320570.2:c.522A>T	NP_001307499.1:p.Ala174=