Canonical Allele Identifier: CA2541175196

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621477_58621478insCC , CM000677.2:g.58621477_58621478insCC	GRCh38
NC_000015.9:g.58913676_58913677insCC , CM000677.1:g.58913676_58913677insCC	GRCh37
NC_000015.8:g.56700968_56700969insCC	NCBI36
NG_033876.1:g.133501_133502insGG
NG_033876.2:g.133230_133231insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1504_1505insGG MANE Select	ENSP00000260408.3:p.Gln502ArgfsTer?
ENST00000260408.7:c.1504_1505insGG	ENSP00000260408.3:p.Gln502ArgfsTer?
ENST00000396136.6:c.1330_1331insGG
ENST00000402627.5:c.154+11837_154+11838insGG	ENSP00000386056.1:n.154+11837_154+11838in...
ENST00000462061.1:n.64_65insGG
ENST00000470269.5:n.33_34insGG
ENST00000475898.1:n.529_530insGG
ENST00000481164.1:n.27_28insGG
ENST00000482945.5:n.27_28insGG
ENST00000561288.1:c.56-23960_56-23959insGG	ENSP00000452639.1:n.56-23960_56-23959insG...
NM_001110.3:c.1504_1505insGG	NP_001101.1:p.Gln502ArgfsTer?
XM_005254117.2:c.1411_1412insGG	XP_005254174.1:p.Gln471ArgfsTer?
NM_001320570.1:c.1411_1412insGG	NP_001307499.1:p.Gln471ArgfsTer?
XM_024449818.1:c.1282_1283insGG	XP_024305586.1:p.Gln428ArgfsTer?
NM_001110.4:c.1504_1505insGG MANE Select	NP_001101.1:p.Gln502ArgfsTer?
NM_001320570.2:c.1411_1412insGG	NP_001307499.1:p.Gln471ArgfsTer?