Canonical Allele Identifier: CA392614624

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58599724C>T , CM000677.2:g.58599724C>T	GRCh38
NC_000015.9:g.58891923C>T , CM000677.1:g.58891923C>T	GRCh37
NC_000015.8:g.56679215C>T	NCBI36
NG_033876.1:g.155255G>A
NG_033876.2:g.154984G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110.4:c.2026G>A MANE Select	NP_001101.1:p.Ala676Thr
ENST00000260408.8:c.2026G>A MANE Select	ENSP00000260408.3:p.Ala676Thr
NM_001110.3:c.2026G>A	NP_001101.1:p.Ala676Thr
NM_001320570.1:c.1933G>A	NP_001307499.1:p.Ala645Thr
NM_001320570.2:c.1933G>A	NP_001307499.1:p.Ala645Thr
ENST00000260408.7:c.2026G>A	ENSP00000260408.3:p.Ala676Thr
ENST00000396136.6:c.1852G>A
ENST00000402627.5:c.155-2206G>A	ENSP00000386056.1:n.155-2206G>A
ENST00000482945.5:n.1730G>A
ENST00000561288.1:c.56-2206G>A	ENSP00000452639.1:n.56-2206G>A
XM_005254117.2:c.1933G>A	XP_005254174.1:p.Ala645Thr
XM_024449818.1:c.1804G>A	XP_024305586.1:p.Ala602Thr