Canonical Allele Identifier: CA490492320

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957362A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665163A>G , CM000677.2:g.58665163A>G	GRCh38
NC_000015.9:g.58957362A>G , CM000677.1:g.58957362A>G	GRCh37
NC_000015.8:g.56744654A>G	NCBI36
NG_033876.1:g.89816T>C
NG_033876.2:g.89545T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.519T>C MANE Select	ENSP00000260408.3:p.Cys173=
ENST00000260408.7:c.519T>C	ENSP00000260408.3:p.Cys173=
ENST00000396136.6:c.345T>C
ENST00000402627.5:c.56-24333T>C	ENSP00000386056.1:n.56-24333T>C
ENST00000439637.5:c.360T>C	ENSP00000391930.1:p.Cys120=
ENST00000497846.5:n.636T>C
ENST00000558733.5:n.755T>C
ENST00000559053.1:c.56-24333T>C	ENSP00000453952.1:n.56-24333T>C
ENST00000561288.1:c.56-67645T>C	ENSP00000452639.1:n.56-67645T>C
NM_001110.3:c.519T>C	NP_001101.1:p.Cys173=
XM_005254117.2:c.519T>C	XP_005254174.1:p.Cys173=
NM_001320570.1:c.519T>C	NP_001307499.1:p.Cys173=
XM_024449818.1:c.297T>C	XP_024305586.1:p.Cys99=
NM_001110.4:c.519T>C MANE Select	NP_001101.1:p.Cys173=
NM_001320570.2:c.519T>C	NP_001307499.1:p.Cys173=