Canonical Allele Identifier: CA2575741275

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58621404-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621404A>T , CM000677.2:g.58621404A>T	GRCh38
NC_000015.9:g.58913603A>T , CM000677.1:g.58913603A>T	GRCh37
NC_000015.8:g.56700895A>T	NCBI36
NG_033876.1:g.133575T>A
NG_033876.2:g.133304T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+67T>A MANE Select	ENSP00000260408.3:n.1511+67T>A
ENST00000260408.7:c.1511+67T>A	ENSP00000260408.3:n.1511+67T>A
ENST00000396136.6:c.1337+67T>A
ENST00000402627.5:c.154+11911T>A	ENSP00000386056.1:n.154+11911T>A
ENST00000462061.1:n.71+67T>A
ENST00000470269.5:n.40+67T>A
ENST00000475898.1:n.536+67T>A
ENST00000481164.1:n.34+67T>A
ENST00000482945.5:n.34+67T>A
ENST00000561288.1:c.56-23886T>A	ENSP00000452639.1:n.56-23886T>A
NM_001110.3:c.1511+67T>A	NP_001101.1:n.1511+67T>A
XM_005254117.2:c.1418+67T>A	XP_005254174.1:n.1418+67T>A
NM_001320570.1:c.1418+67T>A	NP_001307499.1:n.1418+67T>A
XM_024449818.1:c.1289+67T>A	XP_024305586.1:n.1289+67T>A
NM_001110.4:c.1511+67T>A MANE Select	NP_001101.1:n.1511+67T>A
NM_001320570.2:c.1418+67T>A	NP_001307499.1:n.1418+67T>A