Canonical Allele Identifier: CA2628685912

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58621382-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621382T>G , CM000677.2:g.58621382T>G	GRCh38
NC_000015.9:g.58913581T>G , CM000677.1:g.58913581T>G	GRCh37
NC_000015.8:g.56700873T>G	NCBI36
NG_033876.1:g.133597A>C
NG_033876.2:g.133326A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+89A>C MANE Select	ENSP00000260408.3:n.1511+89A>C
ENST00000260408.7:c.1511+89A>C	ENSP00000260408.3:n.1511+89A>C
ENST00000396136.6:c.1337+89A>C
ENST00000402627.5:c.154+11933A>C	ENSP00000386056.1:n.154+11933A>C
ENST00000462061.1:n.71+89A>C
ENST00000470269.5:n.40+89A>C
ENST00000475898.1:n.536+89A>C
ENST00000481164.1:n.34+89A>C
ENST00000482945.5:n.34+89A>C
ENST00000561288.1:c.56-23864A>C	ENSP00000452639.1:n.56-23864A>C
NM_001110.3:c.1511+89A>C	NP_001101.1:n.1511+89A>C
XM_005254117.2:c.1418+89A>C	XP_005254174.1:n.1418+89A>C
NM_001320570.1:c.1418+89A>C	NP_001307499.1:n.1418+89A>C
XM_024449818.1:c.1289+89A>C	XP_024305586.1:n.1289+89A>C
NM_001110.4:c.1511+89A>C MANE Select	NP_001101.1:n.1511+89A>C
NM_001320570.2:c.1418+89A>C	NP_001307499.1:n.1418+89A>C