Canonical Allele Identifier: CA2628685378

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610795-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610795T>A , CM000677.2:g.58610795T>A	GRCh38
NC_000015.9:g.58902994T>A , CM000677.1:g.58902994T>A	GRCh37
NC_000015.8:g.56690286T>A	NCBI36
NG_033876.1:g.144184A>T
NG_033876.2:g.143913A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+204A>T MANE Select	ENSP00000260408.3:n.1804+204A>T
ENST00000260408.7:c.1804+204A>T	ENSP00000260408.3:n.1804+204A>T
ENST00000396136.6:c.1630+204A>T
ENST00000402627.5:c.155-13277A>T	ENSP00000386056.1:n.155-13277A>T
ENST00000470269.5:n.333+204A>T
ENST00000482945.5:n.1231A>T
ENST00000561288.1:c.56-13277A>T	ENSP00000452639.1:n.56-13277A>T
NM_001110.3:c.1804+204A>T	NP_001101.1:n.1804+204A>T
XM_005254117.2:c.1711+204A>T	XP_005254174.1:n.1711+204A>T
NM_001320570.1:c.1711+204A>T	NP_001307499.1:n.1711+204A>T
XM_024449818.1:c.1582+204A>T	XP_024305586.1:n.1582+204A>T
NM_001110.4:c.1804+204A>T MANE Select	NP_001101.1:n.1804+204A>T
NM_001320570.2:c.1711+204A>T	NP_001307499.1:n.1711+204A>T