Canonical Allele Identifier: CA970319581

Gene: ADAM10

Linked Data

• dbSNP Id: rs1895782134
• gnomAD v3: 15-58621380-T-G
• gnomAD v4: 15-58621380-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621380T>G , CM000677.2:g.58621380T>G	GRCh38
NC_000015.9:g.58913579T>G , CM000677.1:g.58913579T>G	GRCh37
NC_000015.8:g.56700871T>G	NCBI36
NG_033876.1:g.133599A>C
NG_033876.2:g.133328A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+91A>C MANE Select	ENSP00000260408.3:n.1511+91A>C
ENST00000260408.7:c.1511+91A>C	ENSP00000260408.3:n.1511+91A>C
ENST00000396136.6:c.1337+91A>C
ENST00000402627.5:c.154+11935A>C	ENSP00000386056.1:n.154+11935A>C
ENST00000462061.1:n.71+91A>C
ENST00000470269.5:n.40+91A>C
ENST00000475898.1:n.536+91A>C
ENST00000481164.1:n.34+91A>C
ENST00000482945.5:n.34+91A>C
ENST00000561288.1:c.56-23862A>C	ENSP00000452639.1:n.56-23862A>C
NM_001110.3:c.1511+91A>C	NP_001101.1:n.1511+91A>C
XM_005254117.2:c.1418+91A>C	XP_005254174.1:n.1418+91A>C
NM_001320570.1:c.1418+91A>C	NP_001307499.1:n.1418+91A>C
XM_024449818.1:c.1289+91A>C	XP_024305586.1:n.1289+91A>C
NM_001110.4:c.1511+91A>C MANE Select	NP_001101.1:n.1511+91A>C
NM_001320570.2:c.1418+91A>C	NP_001307499.1:n.1418+91A>C