Canonical Allele Identifier: CA490492315

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957350T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665151T>G , CM000677.2:g.58665151T>G	GRCh38
NC_000015.9:g.58957350T>G , CM000677.1:g.58957350T>G	GRCh37
NC_000015.8:g.56744642T>G	NCBI36
NG_033876.1:g.89828A>C
NG_033876.2:g.89557A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.531A>C MANE Select	ENSP00000260408.3:p.Ser177=
ENST00000260408.7:c.531A>C	ENSP00000260408.3:p.Ser177=
ENST00000396136.6:c.357A>C
ENST00000402627.5:c.56-24321A>C	ENSP00000386056.1:n.56-24321A>C
ENST00000439637.5:c.372A>C	ENSP00000391930.1:p.Ser124=
ENST00000558733.5:n.767A>C
ENST00000559053.1:c.56-24321A>C	ENSP00000453952.1:n.56-24321A>C
ENST00000561288.1:c.56-67633A>C	ENSP00000452639.1:n.56-67633A>C
NM_001110.3:c.531A>C	NP_001101.1:p.Ser177=
XM_005254117.2:c.531A>C	XP_005254174.1:p.Ser177=
NM_001320570.1:c.531A>C	NP_001307499.1:p.Ser177=
XM_024449818.1:c.309A>C	XP_024305586.1:p.Ser103=
NM_001110.4:c.531A>C MANE Select	NP_001101.1:p.Ser177=
NM_001320570.2:c.531A>C	NP_001307499.1:p.Ser177=