Canonical Allele Identifier: CA2628685318

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610708-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610708G>T , CM000677.2:g.58610708G>T	GRCh38
NC_000015.9:g.58902907G>T , CM000677.1:g.58902907G>T	GRCh37
NC_000015.8:g.56690199G>T	NCBI36
NG_033876.1:g.144271C>A
NG_033876.2:g.144000C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1805-191C>A MANE Select	ENSP00000260408.3:n.1805-191C>A
ENST00000260408.7:c.1805-191C>A	ENSP00000260408.3:n.1805-191C>A
ENST00000396136.6:c.1631-191C>A
ENST00000402627.5:c.155-13190C>A	ENSP00000386056.1:n.155-13190C>A
ENST00000470269.5:n.334-191C>A
ENST00000482945.5:n.1318C>A
ENST00000561288.1:c.56-13190C>A	ENSP00000452639.1:n.56-13190C>A
NM_001110.3:c.1805-191C>A	NP_001101.1:n.1805-191C>A
XM_005254117.2:c.1712-191C>A	XP_005254174.1:n.1712-191C>A
NM_001320570.1:c.1712-191C>A	NP_001307499.1:n.1712-191C>A
XM_024449818.1:c.1583-191C>A	XP_024305586.1:n.1583-191C>A
NM_001110.4:c.1805-191C>A MANE Select	NP_001101.1:n.1805-191C>A
NM_001320570.2:c.1712-191C>A	NP_001307499.1:n.1712-191C>A