Canonical Allele Identifier: CA392621880

Gene: ADAM10

Linked Data

• COSMIC: COSM5462469
• MyVariant Identifiers: chr15:g.58957360G>A (hg19) ; chr15:g.58665161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665161G>A , CM000677.2:g.58665161G>A	GRCh38
NC_000015.9:g.58957360G>A , CM000677.1:g.58957360G>A	GRCh37
NC_000015.8:g.56744652G>A	NCBI36
NG_033876.1:g.89818C>T
NG_033876.2:g.89547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.521C>T MANE Select	ENSP00000260408.3:p.Ala174Val
ENST00000260408.7:c.521C>T	ENSP00000260408.3:p.Ala174Val
ENST00000396136.6:c.347C>T
ENST00000402627.5:c.56-24331C>T	ENSP00000386056.1:n.56-24331C>T
ENST00000439637.5:c.362C>T	ENSP00000391930.1:p.Ala121Val
ENST00000497846.5:n.638C>T
ENST00000558733.5:n.757C>T
ENST00000559053.1:c.56-24331C>T	ENSP00000453952.1:n.56-24331C>T
ENST00000561288.1:c.56-67643C>T	ENSP00000452639.1:n.56-67643C>T
NM_001110.3:c.521C>T	NP_001101.1:p.Ala174Val
XM_005254117.2:c.521C>T	XP_005254174.1:p.Ala174Val
NM_001320570.1:c.521C>T	NP_001307499.1:p.Ala174Val
XM_024449818.1:c.299C>T	XP_024305586.1:p.Ala100Val
NM_001110.4:c.521C>T MANE Select	NP_001101.1:p.Ala174Val
NM_001320570.2:c.521C>T	NP_001307499.1:p.Ala174Val