Canonical Allele Identifier: CA2180476227

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665061_58665062delinsCA , CM000677.2:g.58665061_58665062delinsCA	GRCh38
NC_000015.9:g.58957260_58957261delinsCA , CM000677.1:g.58957260_58957261delinsCA	GRCh37
NC_000015.8:g.56744552_56744553delinsCA	NCBI36
NG_033876.1:g.89917_89918delinsTG
NG_033876.2:g.89646_89647delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+35_585+36delinsTG MANE Select	ENSP00000260408.3:n.585+35_585+36delinsTG
ENST00000260408.7:c.585+35_585+36delinsTG	ENSP00000260408.3:n.585+35_585+36delinsTG
ENST00000396136.6:c.411+35_411+36delinsTG
ENST00000402627.5:c.56-24232_56-24231delinsTG	ENSP00000386056.1:n.56-24232_56-24231delinsTG
ENST00000558733.5:n.821+35_821+36delinsTG
ENST00000559053.1:c.56-24232_56-24231delinsTG	ENSP00000453952.1:n.56-24232_56-24231delinsTG
ENST00000561288.1:c.56-67544_56-67543delinsTG	ENSP00000452639.1:n.56-67544_56-67543delinsTG
NM_001110.3:c.585+35_585+36delinsTG	NP_001101.1:n.585+35_585+36delinsTG
XM_005254117.2:c.585+35_585+36delinsTG	XP_005254174.1:n.585+35_585+36delinsTG
NM_001320570.1:c.585+35_585+36delinsTG	NP_001307499.1:n.585+35_585+36delinsTG
XM_024449818.1:c.363+35_363+36delinsTG	XP_024305586.1:n.363+35_363+36delinsTG
NM_001110.4:c.585+35_585+36delinsTG MANE Select	NP_001101.1:n.585+35_585+36delinsTG
NM_001320570.2:c.585+35_585+36delinsTG	NP_001307499.1:n.585+35_585+36delinsTG