Canonical Allele Identifier: CA392621897

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957361C>T (hg19) ; chr15:g.58665162C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665162C>T , CM000677.2:g.58665162C>T	GRCh38
NC_000015.9:g.58957361C>T , CM000677.1:g.58957361C>T	GRCh37
NC_000015.8:g.56744653C>T	NCBI36
NG_033876.1:g.89817G>A
NG_033876.2:g.89546G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.520G>A MANE Select	ENSP00000260408.3:p.Ala174Thr
ENST00000260408.7:c.520G>A	ENSP00000260408.3:p.Ala174Thr
ENST00000396136.6:c.346G>A
ENST00000402627.5:c.56-24332G>A	ENSP00000386056.1:n.56-24332G>A
ENST00000439637.5:c.361G>A	ENSP00000391930.1:p.Ala121Thr
ENST00000497846.5:n.637G>A
ENST00000558733.5:n.756G>A
ENST00000559053.1:c.56-24332G>A	ENSP00000453952.1:n.56-24332G>A
ENST00000561288.1:c.56-67644G>A	ENSP00000452639.1:n.56-67644G>A
NM_001110.3:c.520G>A	NP_001101.1:p.Ala174Thr
XM_005254117.2:c.520G>A	XP_005254174.1:p.Ala174Thr
NM_001320570.1:c.520G>A	NP_001307499.1:p.Ala174Thr
XM_024449818.1:c.298G>A	XP_024305586.1:p.Ala100Thr
NM_001110.4:c.520G>A MANE Select	NP_001101.1:p.Ala174Thr
NM_001320570.2:c.520G>A	NP_001307499.1:p.Ala174Thr