Canonical Allele Identifier: CA2628685380

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610797-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610797G>A , CM000677.2:g.58610797G>A	GRCh38
NC_000015.9:g.58902996G>A , CM000677.1:g.58902996G>A	GRCh37
NC_000015.8:g.56690288G>A	NCBI36
NG_033876.1:g.144182C>T
NG_033876.2:g.143911C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+202C>T MANE Select	ENSP00000260408.3:n.1804+202C>T
ENST00000260408.7:c.1804+202C>T	ENSP00000260408.3:n.1804+202C>T
ENST00000396136.6:c.1630+202C>T
ENST00000402627.5:c.155-13279C>T	ENSP00000386056.1:n.155-13279C>T
ENST00000470269.5:n.333+202C>T
ENST00000482945.5:n.1229C>T
ENST00000561288.1:c.56-13279C>T	ENSP00000452639.1:n.56-13279C>T
NM_001110.3:c.1804+202C>T	NP_001101.1:n.1804+202C>T
XM_005254117.2:c.1711+202C>T	XP_005254174.1:n.1711+202C>T
NM_001320570.1:c.1711+202C>T	NP_001307499.1:n.1711+202C>T
XM_024449818.1:c.1582+202C>T	XP_024305586.1:n.1582+202C>T
NM_001110.4:c.1804+202C>T MANE Select	NP_001101.1:n.1804+202C>T
NM_001320570.2:c.1711+202C>T	NP_001307499.1:n.1711+202C>T